US20080125778A1 - Method for fixing an augmenter for vertebral body reconstruction - Google Patents

Method for fixing an augmenter for vertebral body reconstruction Download PDF

Info

Publication number
US20080125778A1
US20080125778A1 US11/599,305 US59930506A US2008125778A1 US 20080125778 A1 US20080125778 A1 US 20080125778A1 US 59930506 A US59930506 A US 59930506A US 2008125778 A1 US2008125778 A1 US 2008125778A1
Authority
US
United States
Prior art keywords
augmenter
fixing
vertebral body
vertebral
fixing hole
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/599,305
Inventor
Kung-Chia Li
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US10/957,717 priority Critical patent/US7500992B2/en
Priority to CA002487227A priority patent/CA2487227A1/en
Priority to EP04027434A priority patent/EP1658830A1/en
Application filed by Individual filed Critical Individual
Priority to US11/599,305 priority patent/US20080125778A1/en
Publication of US20080125778A1 publication Critical patent/US20080125778A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/02Surgical instruments, devices or methods, e.g. tourniquets for holding wounds open; Tractors
    • A61B17/025Joint distractors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/70Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/88Osteosynthesis instruments; Methods or means for implanting or extracting internal or external fixation devices
    • A61B17/885Tools for expanding or compacting bones or discs or cavities therein
    • A61B17/8852Tools for expanding or compacting bones or discs or cavities therein capable of being assembled or enlarged, or changing shape, inside the bone or disc
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/70Spinal positioners or stabilisers ; Bone stabilisers comprising fluid filler in an implant
    • A61B17/7001Screws or hooks combined with longitudinal elements which do not contact vertebrae
    • A61B17/7035Screws or hooks, wherein a rod-clamping part and a bone-anchoring part can pivot relative to each other
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/02Surgical instruments, devices or methods, e.g. tourniquets for holding wounds open; Tractors
    • A61B17/025Joint distractors
    • A61B2017/0256Joint distractors for the spine

Definitions

  • the present invention relates to a method for fixing an augmenter for vertebral body reconstruction, more particularly one, according to which an augmenter can be inserted in and firmly joined to a collapsed section of a vertebra so as to enlarge the collapsed vertebral section and restore the vertebra to its original position.
  • Osteoporosis is a disease in which calcium content of bones gradually decreases, and in turns, bones become fragile and more likely to break. If not prevented or if left untreated, osteoporosis can progress to make bones become subject to breakage. Breakage of bones related to osteoporosis usually occurs in the spine.
  • Estrogen deficiency as a result of menopause, especially early or surgically induced in women or low testosterone levels in men; and 6 . Being female and/or having a small frame; females who have never given birth to babies or had their first menstrual period at older age.
  • a conventional method of treating osteoporosis-related fracture is to insert steel nail into a vertebra from rear side of the vertebra. This method has the following disadvantages:
  • a vertebra which has fractured due to osteoporosis, is likely to become unsteady and fracture again after restoration of position with steel nails.
  • a relatively large incision has to be formed on the patient's back, and it takes relatively much time to perform the surgery and for the incision to heal, and the incision is prone to become infected.
  • Another conventional method of treating osteoporosis-related fracture is to insert steel nail into a vertebra from front side of the vertebra. This method has the following disadvantages:
  • Surgical equipments will have to be passed through thoracic cavity or abdominal cavity of the patient in operation therefore nearby organs, e.g. lungs and blood vessels, could be at risk.
  • the method of the present invention includes the following steps: incising a middle of a portion of a rear side of a person's body that faces a collapsed section of a vertebra; establishing a correct position for insertion of an augmenter and drilling a fixing hole on a pedicle of said collapsed vertebral section; putting filler such as harvested autogenous bone, artificial bone, and bone cement into said fixing hole; inserting an augmenter into said fixing hole, and filling said fixing hole with filler such as harvested autogenous bone, artificial bone, and bone cement. Therefore, the method of the present invention has the following advantages over the currently existing ones: The incision is relatively small, and will heal in relatively short length of time, and will not become infected. It takes less time to operate and plant the augmenters. There is no risk of the patient's organs and blood vessels getting injured. And, the augmenters won't cause other healthy vertebras to lose the freedom to move.
  • FIG. 1 is a flow chart of the present invention
  • FIG. 2 is a perspective view of the first augmenter for vertebral body reconstruction in the invention
  • FIG. 3 is an exploded perspective view of the second augmenter in the invention
  • FIG. 4 is an exploded perspective view of the third augmenter
  • FIG. 5 is an exploded perspective view of the fourth augmenter
  • FIG. 6 is an exploded perspective view of the fifth augmenter
  • FIG. 7 is a sectional view of the fifth augmenter
  • FIG. 8 is a view taken when the first augmenter is put into use
  • FIG. 9 is a view taken when the second augmenter is put into use
  • FIG. 10 is a view taken when the third augmenter is put into use
  • FIG. 11 is a view taken when the fourth augmenter is put into use
  • FIG. 12 is a view taken when the fifth augmenter is put into use
  • FIG. 13 is a view taken when the first augmenter is put into use ( 2 ),
  • FIG. 14 is a view taken when the second augmenter is put into use ( 2 ).
  • FIG. 15 is a view taken when the fifth augmenter is in use ( 2 ).
  • a method for fixing an augmenter for vertebral body reconstruction includes the following steps:
  • a first preferred embodiment of an augmenter 1 is rectangular, and tapers off from a second end 12 towards a first end 11 thereof, and has a slightly convexly curved shape with a coarse surface for helping bone to grow as well as increasing firmness of connection between the augmenter 1 and the vertebral body 2 .
  • the augmenter 1 has a screw hole 14 extending from the second end 12 towards the first end 11 ; thus, a planting tool can be passed into the screw hole 14 , and joined to the augmenter 1 for helping insert the augmenter 1 into the vertebral body 2 .
  • the augmenter 1 will enlarge the vertebral body 2 after it is inserted in the fixing hole 22 of the vertebral body 2 .
  • a second preferred embodiment of an augmenter 3 consists of upper and lower planted bars 31 and 32 , and a wedge-shaped bar 33 .
  • the upper and the lower planted bars 31 and 32 have a coarse surface.
  • the upper planted bar 31 has an uppermost portion 311 , an insertion portion 312 projecting down from a lower side of the uppermost portion 311 , longitudinal fitting gaps 313 on lateral sides of front and rear ends of the insertion portion 312 , and a convexly curved base portion 314 at a rear end thereof.
  • the upper planted bar 31 has a screw hole 315 on a front end thereof for a tool to be connected to, which tool is used for planting the upper and the lower planted bars 31 and 32 into the vertebral body 2 .
  • the lower planted bar 32 has a holding room 321 , which has an opening facing upwards, for receiving the insertion portion 312 of the upper planted bar 31 .
  • the lower planted bar 32 has first and second openings 322 and 323 on front and rear ends respectively; the first opening 322 has a T-shape, and the second opening 323 has an U-shape.
  • the lower planted bar 32 has lateral portions 324 on two sides of the first opening 322 and on two sides of the second opening 323 , and the lateral portions 324 will be received in the fitting gaps 313 of the upper planted bar 31 when the upper planted bar 31 is inserted in the lower planted bar 32 .
  • the wedge-shaped bar 33 is inserted in the holding room 321 of the lower planted bar 32 , between the upper and the lower planted bars 31 and 32 , for changing the volume of the whole augmenter 3 .
  • the wedge-shaped bar 33 has a screw hole 331 on a front end thereof for a tool to be connected to.
  • a tool is used to drill a fixing hole 22 on the vertebral section 2 through a pedicle 21 of the vertebral section 2 .
  • the upper planted bar 31 is inserted in the lower planted bar 32 at the insertion portion 312 , and a tool is passed into the screw hole 315 of the upper planted bar 31 , and the upper and the lower planted bars 31 and 32 together are inserted in the fixing hole 22 of the vertebral section 2 with the help of the tool.
  • a tool is passed into the screw hole 331 of the wedge-shaped bar 33 , and the wedge-shaped bar 33 is inserted in the holding room 321 of the lower planted bar 32 , between the upper and the lower planted bars 31 and 32 , with the help of the tool; thus, the upper and the lower planted bars 31 and 32 are propped upwards and downwards respectively by the wedge-shaped bar 33 , thus the vertebral section 2 is propped, and the vertebra restored to its original position.
  • FIG. 4 shows a third preferred embodiment of an augmenter for vertebral body reconstruction in the present invention
  • the upper planted bar 31 of the above-mentioned augmenter 3 is further formed with a concavely curved surface 316 on a lower side of the insertion portion 31 thereof, and the concavely curved surface 316 has several threads 316 a thereon
  • the lower planted bar 32 is further formed with a concavely curved surface 325 on a bottom thereof, which faces the holding room 321 , and the concavely curved surface 325 has several threads 325 a thereon.
  • a threaded element 34 is inserted between the concavely curved surfaces 316 and 325 of the upper and the lower planted bars 31 and 32 to engage the threads 316 a , 325 a ; thus, the upper and the lower planted bars 31 and 32 are propped upwards and downwards respectively by the threaded element 34 , as shown in FIG. 10 .
  • FIG. 5 shows a fourth preferred embodiment of an augmenter for vertebral body reconstruction
  • the lower planted bar 32 of the above-mentioned augmenter 3 is further formed with several holes 326 on a front end thereof for another tool to be connected to, as shown in FIG. 10 .
  • the augmenter 3 can be inserted in a vertebral body more easily with the help of the tool.
  • the wedge-shaped bar 33 further has a downwards sticking extension portion 332 at the front end, which will be stopped by the front end of the lower planted bar 32 when the wedge-shaped bar 33 is inserted in the lower planted bar 32 ; thus, the front ends of the upper planted bar 31 and the wedge-shaped bar 33 will be coplanar when the augmenter 3 is put into use, as shown in FIG. 11 .
  • a fifth preferred embodiment of an augmenter 4 consists of an upper planted bar 41 , and a lower planted bar 42 , both of which have a coarse surface.
  • the upper planted bar 41 has an uppermost portion 411 , an insertion portion 412 on a lower side of the uppermost portion 411 , and stopping post portions 414 protruding down from a rear end of the uppermost portion 411 .
  • the insertion portion 412 has a convexly curved lower side 412 a with a parabola-shape, and protruding portions 413 protruding sideways from two lateral sides of a lower end thereof.
  • the lower planted bar 42 has a fitting trench 421 , which has an upward opening as well as a concavely curved lower side 421 a with a parabola-shape.
  • the lower planted bar 42 further has guide grooves 422 next to two sides of a lower end of the fitting trench 421 ; thus, the protruding portions 413 will be received in respective ones of the guide grooves 422 when the insertion portion 412 of the upper planted bar 41 is fitted on the fitting trench 421 .
  • the lower planted bar 42 further has a screw hole 423 on a front end, and holding portions 424 on a rear end for receiving the stopping post portions 414 of the upper planted bar 41 .
  • a tool is used to drill a fixing hole 22 on the vertebral section 2 through a pedicle 21 of the vertebral section 2 .
  • the upper and the lower planted bars 41 and 42 are joined together with the insertion portion 412 of the upper planted bar 41 being fitted on the fitting trench 421 of the lower planted bar 42 , and a tool is passed into the screw hole 423 of the lower planted bar 42 , and the planted bars 41 and 42 together are inserted in the fixing hole 22 of the vertebral section 2 with the help of the tool.
  • the upper planted bar 41 is moved and adjusted in position in relation to the lower planted bar 42 ; because the insertion portion 412 of the upper planted bar 41 is fitted on the fitting trench 421 of the lower planted bar 42 , and the sideways protruding portions 413 are received in the guide grooves 422 , the longitudinal dimension of the whole augmenter 4 will be changed when the upper planted bar 41 is adjusted in position in relation to the lower planted bar 42 . Consequently, the planted bars 41 and 42 are propped upwards and downwards respectively, thus the vertebral section 2 is propped, and the vertebra restored to its original position.
  • a screw system 5 can be applied to both of the vertebral sections next to the damaged vertebral section 2 for helping increase stability of the spine after the augmenter 1 , 3 or 4 of the present invention is planted.
  • the dimension of the augmenters 1 , 3 and 4 is decided according to the vertical cross-section and the height of the pedicle 21 of the vertebral section 2 ; the vertical cross-section of the pedicle 21 is close to a rectangle, and somewhat oval, and the distance between an upper end and a lower end of the pedicle 21 is greater than that between a left side and a right side; the ratio of the height of pedicle 21 to the height of the vertebral section 2 is between 0.5 and 0.6. Therefore, the augmenter can be made with a size near to the pedicle 21 so that at least 50% to 60% of the vertebra 4 is reconstructed.
  • the height of the augmenters (the second, the third, the fourth and the fifth preferred embodiments) will be changed up to 20 or 30% by means of changing the longitudinal dimension of the augmenter, and in turns, the vertebral section 2 can be nearly restored to the original size, which it had before the fracture. Therefore, with the help of the augmenter, the vertebra can be restored to the original position.
  • the augmenters 3 each consists of upper and lower planted bars 31 and 32 , which can be propped upwards and downwards respectively with the help of the wedge-shaped bar 33 to adjust the longitudinal dimension of the augmenter according to needs.
  • the augmenter 3 (the third preferred embodiment) consists of upper and lower planted bars 31 and 32 , which can be propped upwards and downwards respectively to increase the longitudinal dimension of the augmenter with the help of the threaded element 34 .
  • the augmenter (the fifth preferred embodiment) consists of an upper planted bar 31 having a convexly curved lower side with a parabola-shape, and a lower planted bar 32 , which has a concavely curved upper side touching the convexly curved lower side of the upper planted bar 31 ; thus, longitudinal dimension of the augmenter 4 will be changed when the upper planted bar 41 is adjusted in position in relation to the lower planted bar 42 . Therefore, a damaged vertebral section can be restored to its original height and width after one of the augmenters is inserted and adjusted in longitudinal dimension, and bone draft is used to fill up the vertebral section.
  • the augmenters are coarse, having many small protrusions spread out on the surface, stability of connection of bone mass of the vertebral section will increase, and the augmenters can help bone heal. And, the augmenters can be used alone on a collapsed vertebra without having to carry out operation on other healthy vertebras near to the collapsed one, which operation could cause the other healthy vertebras to lose the freedom to move.
  • the augmenters can be used alone on a collapsed vertebra without the need for operation being done on other healthy vertebras near to the collapsed one, which operation would cause damage and loss of freedom of motion to the other healthy vertebras.
  • the augmenters can be adjusted in their longitudinal dimension according to needs after they are inserted in a collapsed vertebra.
  • the augmenters are only inserted in the collapsed vertebra therefore they won't cause other healthy vertebras to lose the freedom to move.

Abstract

A method for fixing an augmenter for vertebral body reconstruction includes following steps: incising a middle of a portion of a rear side of a person's body that faces a collapsed section of a vertebra; establishing a correct position for insertion of an augmenter and drilling a fixing hole on a pedicle of said collapsed vertebral section; putting filler such as harvested autogenous bone, artificial bone, and bone cement into said fixing hole; inserting an augmenter into said fixing hole, and filling said fixing hole with filler such as harvested autogenous bone, artificial bone, and bone cement.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to a method for fixing an augmenter for vertebral body reconstruction, more particularly one, according to which an augmenter can be inserted in and firmly joined to a collapsed section of a vertebra so as to enlarge the collapsed vertebral section and restore the vertebra to its original position.
  • 2. Brief Description of the Prior Art
  • Osteoporosis is a disease in which calcium content of bones gradually decreases, and in turns, bones become fragile and more likely to break. If not prevented or if left untreated, osteoporosis can progress to make bones become subject to breakage. Breakage of bones related to osteoporosis usually occurs in the spine.
  • Certain people are more likely to develop osteoporosis than others. Risk factors have been identified as followings, which will increase the likelihood of developing osteoporosis:
  • 1. Being Caucasian or Asian; average skeletal mass of Caucasian and Asian is lower than that of black people, and Caucasian and Asian are more likely than black people to develop osteoporosis;
  • 2. An improper lifestyle; use of alcohol, cigarette, excessive use of coffee, tea, and excessive or lack of exercises;
  • 3. A family history of osteoporosis;
  • 4. Use of certain medications, such as corticosteroids, and anticonvulsants;
  • 5. Estrogen deficiency as a result of menopause, especially early or surgically induced in women or low testosterone levels in men; and 6. Being female and/or having a small frame; females who have never given birth to babies or had their first menstrual period at older age.
  • A conventional method of treating osteoporosis-related fracture is to insert steel nail into a vertebra from rear side of the vertebra. This method has the following disadvantages:
  • 1. Two vertebras above the fractured vertebra and two under the fractured vertebra have to be fixed if this method is used. Consequently, a big portion of the spine becomes stiff, flexibility of the spine is reduced to a large degree.
  • 2. A vertebra, which has fractured due to osteoporosis, is likely to become unsteady and fracture again after restoration of position with steel nails.
  • 3. A relatively large incision has to be formed on the patient's back, and it takes relatively much time to perform the surgery and for the incision to heal, and the incision is prone to become infected.
  • Another conventional method of treating osteoporosis-related fracture is to insert steel nail into a vertebra from front side of the vertebra. This method has the following disadvantages:
  • 1. Surgical equipments will have to be passed through thoracic cavity or abdominal cavity of the patient in operation therefore nearby organs, e.g. lungs and blood vessels, could be at risk.
  • 2. It takes relatively much time to perform the surgery. And, there is risk of infection because donated bones or ribs of the patient from front side of the vertebra will be used according to this method.
  • 3. It also will cause reduction of the flexibility of the spine.
  • SUMMARY OF THE INVENTION
  • It is a main object of the invention to provide an improvement on a method for fixing an augmenter for vertebral body reconstruction to overcome the above-mentioned problems.
  • The method of the present invention includes the following steps: incising a middle of a portion of a rear side of a person's body that faces a collapsed section of a vertebra; establishing a correct position for insertion of an augmenter and drilling a fixing hole on a pedicle of said collapsed vertebral section; putting filler such as harvested autogenous bone, artificial bone, and bone cement into said fixing hole; inserting an augmenter into said fixing hole, and filling said fixing hole with filler such as harvested autogenous bone, artificial bone, and bone cement. Therefore, the method of the present invention has the following advantages over the currently existing ones: The incision is relatively small, and will heal in relatively short length of time, and will not become infected. It takes less time to operate and plant the augmenters. There is no risk of the patient's organs and blood vessels getting injured. And, the augmenters won't cause other healthy vertebras to lose the freedom to move.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The present invention will be better understood by referring to the accompanying drawings, wherein:
  • FIG. 1 is a flow chart of the present invention,
  • FIG. 2 is a perspective view of the first augmenter for vertebral body reconstruction in the invention,
  • FIG. 3 is an exploded perspective view of the second augmenter in the invention,
  • FIG. 4 is an exploded perspective view of the third augmenter,
  • FIG. 5 is an exploded perspective view of the fourth augmenter,
  • FIG. 6 is an exploded perspective view of the fifth augmenter,
  • FIG. 7 is a sectional view of the fifth augmenter,
  • FIG. 8 is a view taken when the first augmenter is put into use,
  • FIG. 9 is a view taken when the second augmenter is put into use,
  • FIG. 10 is a view taken when the third augmenter is put into use,
  • FIG. 11 is a view taken when the fourth augmenter is put into use,
  • FIG. 12 is a view taken when the fifth augmenter is put into use,
  • FIG. 13 is a view taken when the first augmenter is put into use (2),
  • FIG. 14 is a view taken when the second augmenter is put into use (2), and
  • FIG. 15 is a view taken when the fifth augmenter is in use (2).
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Referring to FIG. 1, a method for fixing an augmenter for vertebral body reconstruction includes the following steps:
  • (a) We find out which section of a vertebral body 2 is damaged (collapsed), and incise a middle of a portion of a rear side of the patient's body that faces the damaged vertebral section, and we peel off the soft tissues, and separate the vertebral bows, small-faced joints, and transverse processes;
  • (b) We establish the correct position for insertion of the augmenter with the help of a C-arm fluoroscopy, and drill a fixing hole 22 on the damaged vertebral section 2, through a pedicle 21 of the section 2;
  • (c) We enlarge the image of the fixing hole 22 for following fixing actions by means of a magnifier;
  • (d) We put filler such as harvested autogenous bone, artificial bone, and bone cement into the fixing hole 22;
  • (e) We insert an augmenter 1, 3 or 4 into the fixing hole 22, and establish that the augmenter 1, 3, 4 is in the correct position by means of a C-arm fluoroscopy;
  • (f) Finally, we fill the fixing hole 22 with filler such as harvested autogenous bone, artificial bone, and bone cement so as to level out the vertebral body 2 and prevent the augmenter 1, 3, 4 from falling off.
  • Referring to FIG. 2, a first preferred embodiment of an augmenter 1 is rectangular, and tapers off from a second end 12 towards a first end 11 thereof, and has a slightly convexly curved shape with a coarse surface for helping bone to grow as well as increasing firmness of connection between the augmenter 1 and the vertebral body 2. The augmenter 1 has a screw hole 14 extending from the second end 12 towards the first end 11; thus, a planting tool can be passed into the screw hole 14, and joined to the augmenter 1 for helping insert the augmenter 1 into the vertebral body 2. Referring to FIG. 8, the augmenter 1 will enlarge the vertebral body 2 after it is inserted in the fixing hole 22 of the vertebral body 2.
  • Referring to FIG. 3, a second preferred embodiment of an augmenter 3 consists of upper and lower planted bars 31 and 32, and a wedge-shaped bar 33. The upper and the lower planted bars 31 and 32 have a coarse surface. The upper planted bar 31 has an uppermost portion 311, an insertion portion 312 projecting down from a lower side of the uppermost portion 311, longitudinal fitting gaps 313 on lateral sides of front and rear ends of the insertion portion 312, and a convexly curved base portion 314 at a rear end thereof. Furthermore, the upper planted bar 31 has a screw hole 315 on a front end thereof for a tool to be connected to, which tool is used for planting the upper and the lower planted bars 31 and 32 into the vertebral body 2.
  • The lower planted bar 32 has a holding room 321, which has an opening facing upwards, for receiving the insertion portion 312 of the upper planted bar 31. The lower planted bar 32 has first and second openings 322 and 323 on front and rear ends respectively; the first opening 322 has a T-shape, and the second opening 323 has an U-shape. The lower planted bar 32 has lateral portions 324 on two sides of the first opening 322 and on two sides of the second opening 323, and the lateral portions 324 will be received in the fitting gaps 313 of the upper planted bar 31 when the upper planted bar 31 is inserted in the lower planted bar 32.
  • The wedge-shaped bar 33 is inserted in the holding room 321 of the lower planted bar 32, between the upper and the lower planted bars 31 and 32, for changing the volume of the whole augmenter 3. In addition, the wedge-shaped bar 33 has a screw hole 331 on a front end thereof for a tool to be connected to.
  • Referring to FIG. 9, to plant the augmenter 3 into a damaged vertebral section 2, first a tool is used to drill a fixing hole 22 on the vertebral section 2 through a pedicle 21 of the vertebral section 2. Second, the upper planted bar 31 is inserted in the lower planted bar 32 at the insertion portion 312, and a tool is passed into the screw hole 315 of the upper planted bar 31, and the upper and the lower planted bars 31 and 32 together are inserted in the fixing hole 22 of the vertebral section 2 with the help of the tool. Next, a tool is passed into the screw hole 331 of the wedge-shaped bar 33, and the wedge-shaped bar 33 is inserted in the holding room 321 of the lower planted bar 32, between the upper and the lower planted bars 31 and 32, with the help of the tool; thus, the upper and the lower planted bars 31 and 32 are propped upwards and downwards respectively by the wedge-shaped bar 33, thus the vertebral section 2 is propped, and the vertebra restored to its original position.
  • FIG. 4 shows a third preferred embodiment of an augmenter for vertebral body reconstruction in the present invention; the upper planted bar 31 of the above-mentioned augmenter 3 is further formed with a concavely curved surface 316 on a lower side of the insertion portion 31 thereof, and the concavely curved surface 316 has several threads 316 a thereon; the lower planted bar 32 is further formed with a concavely curved surface 325 on a bottom thereof, which faces the holding room 321, and the concavely curved surface 325 has several threads 325 a thereon. In use, a threaded element 34 is inserted between the concavely curved surfaces 316 and 325 of the upper and the lower planted bars 31 and 32 to engage the threads 316 a, 325 a; thus, the upper and the lower planted bars 31 and 32 are propped upwards and downwards respectively by the threaded element 34, as shown in FIG. 10.
  • FIG. 5 shows a fourth preferred embodiment of an augmenter for vertebral body reconstruction; the lower planted bar 32 of the above-mentioned augmenter 3 is further formed with several holes 326 on a front end thereof for another tool to be connected to, as shown in FIG. 10. Thus, the augmenter 3 can be inserted in a vertebral body more easily with the help of the tool. And, the wedge-shaped bar 33 further has a downwards sticking extension portion 332 at the front end, which will be stopped by the front end of the lower planted bar 32 when the wedge-shaped bar 33 is inserted in the lower planted bar 32; thus, the front ends of the upper planted bar 31 and the wedge-shaped bar 33 will be coplanar when the augmenter 3 is put into use, as shown in FIG. 11.
  • Referring to FIGS. 6 and 7, a fifth preferred embodiment of an augmenter 4 consists of an upper planted bar 41, and a lower planted bar 42, both of which have a coarse surface.
  • The upper planted bar 41 has an uppermost portion 411, an insertion portion 412 on a lower side of the uppermost portion 411, and stopping post portions 414 protruding down from a rear end of the uppermost portion 411. The insertion portion 412 has a convexly curved lower side 412 a with a parabola-shape, and protruding portions 413 protruding sideways from two lateral sides of a lower end thereof.
  • The lower planted bar 42 has a fitting trench 421, which has an upward opening as well as a concavely curved lower side 421 a with a parabola-shape. The lower planted bar 42 further has guide grooves 422 next to two sides of a lower end of the fitting trench 421; thus, the protruding portions 413 will be received in respective ones of the guide grooves 422 when the insertion portion 412 of the upper planted bar 41 is fitted on the fitting trench 421. The lower planted bar 42 further has a screw hole 423 on a front end, and holding portions 424 on a rear end for receiving the stopping post portions 414 of the upper planted bar 41.
  • Referring to FIG. 12, to plant the augmenter 4 into a damaged vertebral section 2, first a tool is used to drill a fixing hole 22 on the vertebral section 2 through a pedicle 21 of the vertebral section 2. Second, the upper and the lower planted bars 41 and 42 are joined together with the insertion portion 412 of the upper planted bar 41 being fitted on the fitting trench 421 of the lower planted bar 42, and a tool is passed into the screw hole 423 of the lower planted bar 42, and the planted bars 41 and 42 together are inserted in the fixing hole 22 of the vertebral section 2 with the help of the tool. Next, the upper planted bar 41 is moved and adjusted in position in relation to the lower planted bar 42; because the insertion portion 412 of the upper planted bar 41 is fitted on the fitting trench 421 of the lower planted bar 42, and the sideways protruding portions 413 are received in the guide grooves 422, the longitudinal dimension of the whole augmenter 4 will be changed when the upper planted bar 41 is adjusted in position in relation to the lower planted bar 42. Consequently, the planted bars 41 and 42 are propped upwards and downwards respectively, thus the vertebral section 2 is propped, and the vertebra restored to its original position.
  • Referring to FIGS. 13 to 15, if it is necessary, a screw system 5 can be applied to both of the vertebral sections next to the damaged vertebral section 2 for helping increase stability of the spine after the augmenter 1, 3 or 4 of the present invention is planted.
  • The dimension of the augmenters 1, 3 and 4 is decided according to the vertical cross-section and the height of the pedicle 21 of the vertebral section 2; the vertical cross-section of the pedicle 21 is close to a rectangle, and somewhat oval, and the distance between an upper end and a lower end of the pedicle 21 is greater than that between a left side and a right side; the ratio of the height of pedicle 21 to the height of the vertebral section 2 is between 0.5 and 0.6. Therefore, the augmenter can be made with a size near to the pedicle 21 so that at least 50% to 60% of the vertebra 4 is reconstructed. Consequently, 70% to 80% of the vertebral section 2 will be reconstructed when the augmenter is combined with the remaining bone mass of the damaged vertebral section 2. Furthermore, the height of the augmenters (the second, the third, the fourth and the fifth preferred embodiments) will be changed up to 20 or 30% by means of changing the longitudinal dimension of the augmenter, and in turns, the vertebral section 2 can be nearly restored to the original size, which it had before the fracture. Therefore, with the help of the augmenter, the vertebra can be restored to the original position.
  • Because the above augmenters are planted into a collapsed vertebra through a pedicle of the vertebra instead of via the thoracic or abdominal cavity of the patient therefore the operation is relatively safe as compared with the last conventional way described in the Background, and mechanical strength of the vertebra is increased.
  • The augmenters 3 (the second and the fourth preferred embodiment) each consists of upper and lower planted bars 31 and 32, which can be propped upwards and downwards respectively with the help of the wedge-shaped bar 33 to adjust the longitudinal dimension of the augmenter according to needs. And, the augmenter 3 (the third preferred embodiment) consists of upper and lower planted bars 31 and 32, which can be propped upwards and downwards respectively to increase the longitudinal dimension of the augmenter with the help of the threaded element 34. The augmenter (the fifth preferred embodiment) consists of an upper planted bar 31 having a convexly curved lower side with a parabola-shape, and a lower planted bar 32, which has a concavely curved upper side touching the convexly curved lower side of the upper planted bar 31; thus, longitudinal dimension of the augmenter 4 will be changed when the upper planted bar 41 is adjusted in position in relation to the lower planted bar 42. Therefore, a damaged vertebral section can be restored to its original height and width after one of the augmenters is inserted and adjusted in longitudinal dimension, and bone draft is used to fill up the vertebral section. Furthermore, because the augmenters are coarse, having many small protrusions spread out on the surface, stability of connection of bone mass of the vertebral section will increase, and the augmenters can help bone heal. And, the augmenters can be used alone on a collapsed vertebra without having to carry out operation on other healthy vertebras near to the collapsed one, which operation could cause the other healthy vertebras to lose the freedom to move.
  • From the above description, it can be seen that the present invention has the following advantages:
  • 1. The augmenters can be used alone on a collapsed vertebra without the need for operation being done on other healthy vertebras near to the collapsed one, which operation would cause damage and loss of freedom of motion to the other healthy vertebras.
  • 2. The augmenters can be adjusted in their longitudinal dimension according to needs after they are inserted in a collapsed vertebra.
  • 3. Doctors have to drill a hole on only that section of a vertebra that is collapsed, and the incision is relatively small therefore the incision will heal in relatively short length of time, and will not become infected.
  • 4. It takes less time to operate and plant the augmenters.
  • 5. Because the augmenters are planted from the rear side of the patient's body therefore there is no risk of the patient's organs and blood vessels getting injured.
  • 6. The augmenters are only inserted in the collapsed vertebra therefore they won't cause other healthy vertebras to lose the freedom to move.

Claims (11)

1. A method for fixing an augmenter for vertebral body reconstruction, comprising following steps:
(a) incising a middle of a portion of a rear side of a person's body that faces a collapsed section of a vertebra;
(b) establishing a correct position for insertion of an augmenter and drilling a fixing hole on said collapsed vertebral section, through a pedicle of said collapsed vertebral section;
(c) putting fillers into said fixing hole;
(d) inserting an augmenter into said fixing hole; and
(e) filling said fixing hole with fillers.
2. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein in drilling said fixing hole, the correct position for insertion of the augmenter is established with help of a C-arm fluoroscopy.
3. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein an image of said fixing hole is enlarged by means of a magnifier.
4. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein a C-arm fluoroscopy is used to establish that said augmenter is in the correct position after said augmenter is inserted into said fixing hole.
5. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein a screw system is applied to those of the vertebra that are next to said collapsed vertebral section for increasing healing speed of said vertebra.
6. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein the filler used in step (c) is harvested autogenous bone.
7. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein the filler used in step (c) is artificial bone.
8. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein the filler used in step (c) is bone cement.
9. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 1, wherein the filler used in step (e) is harvested autogenous bone.
10. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 6, wherein the filler used in step (e) is artificial bone.
11. The method for fixing an augmenter for vertebral body reconstruction as recited in claim 6, wherein the filler used in step (e) is bone cement.
US11/599,305 2004-10-05 2006-11-15 Method for fixing an augmenter for vertebral body reconstruction Abandoned US20080125778A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US10/957,717 US7500992B2 (en) 2004-10-05 2004-10-05 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction
CA002487227A CA2487227A1 (en) 2004-10-05 2004-11-10 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction
EP04027434A EP1658830A1 (en) 2004-10-05 2004-11-18 Distractable body augmeter capable of being planted through a pedicle for vertebral body reconstruction
US11/599,305 US20080125778A1 (en) 2004-10-05 2006-11-15 Method for fixing an augmenter for vertebral body reconstruction

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US10/957,717 US7500992B2 (en) 2004-10-05 2004-10-05 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction
CA002487227A CA2487227A1 (en) 2004-10-05 2004-11-10 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction
EP04027434A EP1658830A1 (en) 2004-10-05 2004-11-18 Distractable body augmeter capable of being planted through a pedicle for vertebral body reconstruction
US11/599,305 US20080125778A1 (en) 2004-10-05 2006-11-15 Method for fixing an augmenter for vertebral body reconstruction

Publications (1)

Publication Number Publication Date
US20080125778A1 true US20080125778A1 (en) 2008-05-29

Family

ID=44883444

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/957,717 Expired - Fee Related US7500992B2 (en) 2004-10-05 2004-10-05 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction
US11/599,305 Abandoned US20080125778A1 (en) 2004-10-05 2006-11-15 Method for fixing an augmenter for vertebral body reconstruction

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10/957,717 Expired - Fee Related US7500992B2 (en) 2004-10-05 2004-10-05 Distractable body augmenter capable of being planted through a pedicle for vertebral body reconstruction

Country Status (3)

Country Link
US (2) US7500992B2 (en)
EP (1) EP1658830A1 (en)
CA (1) CA2487227A1 (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9358123B2 (en) 2011-08-09 2016-06-07 Neuropro Spinal Jaxx, Inc. Bone fusion device, apparatus and method
US9526525B2 (en) 2006-08-22 2016-12-27 Neuropro Technologies, Inc. Percutaneous system for dynamic spinal stabilization
US9532883B2 (en) 2012-04-13 2017-01-03 Neuropro Technologies, Inc. Bone fusion device
US9974665B2 (en) 2004-11-03 2018-05-22 Neuropro Technologies, Inc. Bone fusion device
US10098757B2 (en) 2013-03-15 2018-10-16 Neuropro Technologies Inc. Bodiless bone fusion device, apparatus and method
US10111760B2 (en) 2017-01-18 2018-10-30 Neuropro Technologies, Inc. Bone fusion system, device and method including a measuring mechanism
US10159583B2 (en) 2012-04-13 2018-12-25 Neuropro Technologies, Inc. Bone fusion device
US10213321B2 (en) 2017-01-18 2019-02-26 Neuropro Technologies, Inc. Bone fusion system, device and method including delivery apparatus
US10292830B2 (en) 2011-08-09 2019-05-21 Neuropro Technologies, Inc. Bone fusion device, system and method
US10420654B2 (en) 2011-08-09 2019-09-24 Neuropro Technologies, Inc. Bone fusion device, system and method
US10729560B2 (en) 2017-01-18 2020-08-04 Neuropro Technologies, Inc. Bone fusion system, device and method including an insertion instrument
US10973657B2 (en) 2017-01-18 2021-04-13 Neuropro Technologies, Inc. Bone fusion surgical system and method
US11963884B2 (en) 2022-07-25 2024-04-23 Neuropro Technologies, Inc. Bodiless bone fusion device, apparatus and method

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2363254C (en) 1999-03-07 2009-05-05 Discure Ltd. Method and apparatus for computerized surgery
US7875078B2 (en) * 2004-08-25 2011-01-25 Spine Wave, Inc. Expandable interbody fusion device
US20080161929A1 (en) 2006-12-29 2008-07-03 Mccormack Bruce Cervical distraction device
US9005288B2 (en) * 2008-01-09 2015-04-14 Providence Medical Techonlogy, Inc. Methods and apparatus for accessing and treating the facet joint
WO2010030994A2 (en) 2008-06-06 2010-03-18 Providence Medical Technology, Inc. Cervical distraction/implant delivery device
US9333086B2 (en) 2008-06-06 2016-05-10 Providence Medical Technology, Inc. Spinal facet cage implant
WO2009148619A2 (en) 2008-06-06 2009-12-10 Providence Medical Technology, Inc. Facet joint implants and delivery tools
US9381049B2 (en) 2008-06-06 2016-07-05 Providence Medical Technology, Inc. Composite spinal facet implant with textured surfaces
US11224521B2 (en) 2008-06-06 2022-01-18 Providence Medical Technology, Inc. Cervical distraction/implant delivery device
US8361152B2 (en) 2008-06-06 2013-01-29 Providence Medical Technology, Inc. Facet joint implants and delivery tools
US8267966B2 (en) 2008-06-06 2012-09-18 Providence Medical Technology, Inc. Facet joint implants and delivery tools
US9220554B2 (en) 2010-02-18 2015-12-29 Globus Medical, Inc. Methods and apparatus for treating vertebral fractures
US9402744B2 (en) * 2010-06-11 2016-08-02 International Spinal Innovations, Llc Pre-packed corpectomy device to improve fusion
US9144501B1 (en) 2010-07-16 2015-09-29 Nuvasive, Inc. Fracture reduction device and methods
US9358122B2 (en) 2011-01-07 2016-06-07 K2M, Inc. Interbody spacer
US20130178940A1 (en) * 2012-01-06 2013-07-11 Thompson Mis Expandable cage spinal implant
USD732667S1 (en) 2012-10-23 2015-06-23 Providence Medical Technology, Inc. Cage spinal implant
USD745156S1 (en) 2012-10-23 2015-12-08 Providence Medical Technology, Inc. Spinal implant
US9456908B2 (en) 2013-03-12 2016-10-04 Coorstek Medical Llc Fusion cage
WO2015184018A1 (en) 2014-05-28 2015-12-03 Providence Medical Technology, Inc. Lateral mass fixation system
USD841165S1 (en) 2015-10-13 2019-02-19 Providence Medical Technology, Inc. Cervical cage
US10682243B2 (en) 2015-10-13 2020-06-16 Providence Medical Technology, Inc. Spinal joint implant delivery device and system
TW201806562A (en) 2016-06-28 2018-03-01 普羅維登斯醫療科技公司 Spinal implant and methods of using the same
USD887552S1 (en) 2016-07-01 2020-06-16 Providence Medical Technology, Inc. Cervical cage
AU2018229683B2 (en) 2017-03-07 2023-10-12 DSB Co Pty Ltd A surgical device with sensor
JP2020521536A (en) 2017-05-19 2020-07-27 プロビデンス メディカル テクノロジー インコーポレイテッド Spinal fixation access and delivery system
WO2019136263A1 (en) 2018-01-04 2019-07-11 Providence Medical Technology, Inc. Facet screw and delivery device
USD933230S1 (en) 2019-04-15 2021-10-12 Providence Medical Technology, Inc. Cervical cage
USD911525S1 (en) 2019-06-21 2021-02-23 Providence Medical Technology, Inc. Spinal cage
USD945621S1 (en) 2020-02-27 2022-03-08 Providence Medical Technology, Inc. Spinal cage

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE9407806U1 (en) * 1994-05-11 1994-07-14 Aesculap Ag Intervertebral implant
ES2158132T3 (en) * 1995-10-20 2001-09-01 Synthes Ag INTERVERTEBRAL IMPLANT WITH BOX AND ROTATING BODY.
FR2771282B1 (en) * 1997-11-25 2000-01-28 Jean Taylor VERTEBRAL IMPLANT SUITABLE FOR INTRODUCTION BY A POSTERIOR ROUTE IN AN INTERVERTEBRAL SPACE
DE19807236C2 (en) * 1998-02-20 2000-06-21 Biedermann Motech Gmbh Intervertebral implant
FR2782632B1 (en) * 1998-08-28 2000-12-29 Materiel Orthopedique En Abreg EXPANSIBLE INTERSOMATIC FUSION CAGE
US6102950A (en) * 1999-01-19 2000-08-15 Vaccaro; Alex Intervertebral body fusion device
US6491724B1 (en) * 1999-08-13 2002-12-10 Bret Ferree Spinal fusion cage with lordosis correction
WO2002038062A2 (en) * 2000-11-13 2002-05-16 Boehm Frank H Jr Device and method for lumbar interbody fusion
US6454807B1 (en) * 2000-11-30 2002-09-24 Roger P. Jackson Articulated expandable spinal fusion cage system
US6685742B1 (en) * 2002-11-12 2004-02-03 Roger P. Jackson Articulated anterior expandable spinal fusion cage system
US7828849B2 (en) * 2003-02-03 2010-11-09 Warsaw Orthopedic, Inc. Expanding interbody implant and articulating inserter and method

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11583414B2 (en) 2004-11-03 2023-02-21 Neuropro Technologies, Inc. Bone fusion device
US9974665B2 (en) 2004-11-03 2018-05-22 Neuropro Technologies, Inc. Bone fusion device
US10682240B2 (en) 2004-11-03 2020-06-16 Neuropro Technologies, Inc. Bone fusion device
US9526525B2 (en) 2006-08-22 2016-12-27 Neuropro Technologies, Inc. Percutaneous system for dynamic spinal stabilization
US10420654B2 (en) 2011-08-09 2019-09-24 Neuropro Technologies, Inc. Bone fusion device, system and method
US11452616B2 (en) 2011-08-09 2022-09-27 Neuropro Spinal Jaxx, Inc. Bone fusion device, apparatus and method
US10092422B2 (en) 2011-08-09 2018-10-09 Neuropro Spinal Jaxx, Inc. Bone fusion device, apparatus and method
US11432940B2 (en) 2011-08-09 2022-09-06 Neuropro Technologies, Inc. Bone fusion device, system and method
US10736754B2 (en) 2011-08-09 2020-08-11 Neuropro Spinal Jaxx, Inc. Bone fusion device, apparatus and method
US9358123B2 (en) 2011-08-09 2016-06-07 Neuropro Spinal Jaxx, Inc. Bone fusion device, apparatus and method
US10292830B2 (en) 2011-08-09 2019-05-21 Neuropro Technologies, Inc. Bone fusion device, system and method
US10709574B2 (en) 2012-04-13 2020-07-14 Neuropro Technologies, Inc. Bone fusion device
US9532883B2 (en) 2012-04-13 2017-01-03 Neuropro Technologies, Inc. Bone fusion device
US10159583B2 (en) 2012-04-13 2018-12-25 Neuropro Technologies, Inc. Bone fusion device
US10016283B2 (en) 2012-04-13 2018-07-10 Neuropro Technologies, Inc. Bone fusion device
US11439517B2 (en) 2012-04-13 2022-09-13 Neuropro Technologies, Inc. Bone fusion device
US11399956B2 (en) 2013-03-15 2022-08-02 Neuropro Technologies, Inc. Bodiless bone fusion device, apparatus and method
US10575966B2 (en) 2013-03-15 2020-03-03 Neuropro Technologies, Inc. Bodiless bone fusion device, apparatus and method
US10098757B2 (en) 2013-03-15 2018-10-16 Neuropro Technologies Inc. Bodiless bone fusion device, apparatus and method
US10729562B2 (en) 2017-01-18 2020-08-04 Neuropro Technologies, Inc. Bone fusion system, device and method including a measuring mechanism
US11141289B2 (en) 2017-01-18 2021-10-12 Neuropro Technologies, Inc. Bone fusion system, device and method including delivery apparatus
US10973657B2 (en) 2017-01-18 2021-04-13 Neuropro Technologies, Inc. Bone fusion surgical system and method
US10111760B2 (en) 2017-01-18 2018-10-30 Neuropro Technologies, Inc. Bone fusion system, device and method including a measuring mechanism
US10729560B2 (en) 2017-01-18 2020-08-04 Neuropro Technologies, Inc. Bone fusion system, device and method including an insertion instrument
US11458029B2 (en) 2017-01-18 2022-10-04 Neuropro Technologies, Inc. Bone fusion system, device and method including a measuring mechanism
US11497623B2 (en) 2017-01-18 2022-11-15 Neuropro Technologies, Inc. Bone fusion system, device and method including an insertion instrument
US10213321B2 (en) 2017-01-18 2019-02-26 Neuropro Technologies, Inc. Bone fusion system, device and method including delivery apparatus
US11963884B2 (en) 2022-07-25 2024-04-23 Neuropro Technologies, Inc. Bodiless bone fusion device, apparatus and method

Also Published As

Publication number Publication date
CA2487227A1 (en) 2006-05-10
EP1658830A1 (en) 2006-05-24
US20060085007A1 (en) 2006-04-20
US7500992B2 (en) 2009-03-10

Similar Documents

Publication Publication Date Title
US20080125778A1 (en) Method for fixing an augmenter for vertebral body reconstruction
US10130401B2 (en) Growth control device
AU2013273678B2 (en) Ball and socket implants for correction of hammer toes and claw toe
JP3177020U (en) Bone plate around the prosthesis
JP5000485B2 (en) Surgical apparatus and surgical method for wedge osteotomy
MX2011008822A (en) Pediatric long bone support or fixation plate.
US11883038B2 (en) Implants, devices, systems, kits and methods of implanting
US10646263B2 (en) Bunion correction system and method
US20100082068A1 (en) Intramedullary Tubular Bone Fixation
US11000320B2 (en) Medial buttress construct and a fracture fixation device for femoral neck
US20040111090A1 (en) Modification of percutaneous intrafocal plate system
CN112912022A (en) Bone fixation device and system
EP2948072A2 (en) Caps for implants and implant assemblies
KR100811563B1 (en) The minimally invasive instrument of spinal fixation device
EP1609444A1 (en) Implant capable of being implanted through a pedicle for vertebral body reconstruction
Zheng et al. Removal of a broken trigen intertan intertrochanteric antegrade nail
US11224469B2 (en) Implants and related methods for bunion correction
CN211962167U (en) Bone fracture plate
CN108261272B (en) Artificial vertebral canal for preventing spinal nerve compression
CN111281516A (en) Anatomical external fixation steel plate and fixation system for femoral neck fracture
CN217472057U (en) Anatomical form malleolus medialis lockplate
CN214908684U (en) Fusiform is in same direction as fixed type of thorn hook vertebra joint and is fused ware
JP3108284U (en) Spine rehabilitation rehabilitation tool
Reyad et al. Lag Screw in Mandibular Plate Technique for Sagittal Splitting Mandibular Fractures
CN114917005A (en) Inserting wedge type tibial plateau posterolateral cross supporting system and application thereof

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION