US20170007429A1 - Tubular Metal Prosthesis and Method of Making It - Google Patents

Tubular Metal Prosthesis and Method of Making It Download PDF

Info

Publication number
US20170007429A1
US20170007429A1 US15/269,866 US201615269866A US2017007429A1 US 20170007429 A1 US20170007429 A1 US 20170007429A1 US 201615269866 A US201615269866 A US 201615269866A US 2017007429 A1 US2017007429 A1 US 2017007429A1
Authority
US
United States
Prior art keywords
stent
polished
ramp surfaces
head portion
stent body
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
US15/269,866
Inventor
Jaqueline Wolf
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.)
CR Bard Inc
Original Assignee
CR Bard Inc
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
Application filed by CR Bard Inc filed Critical CR Bard Inc
Priority to US15/269,866 priority Critical patent/US20170007429A1/en
Publication of US20170007429A1 publication Critical patent/US20170007429A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/89Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
    • A61F2/915Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K31/00Processes relevant to this subclass, specially adapted for particular articles or purposes, but not covered by only one of the preceding main groups
    • B23K31/02Processes relevant to this subclass, specially adapted for particular articles or purposes, but not covered by only one of the preceding main groups relating to soldering or welding
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
    • A61F2/915Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • A61F2002/9155Adjacent bands being connected to each other
    • A61F2002/91591Locking connectors, e.g. using male-female connections
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/0058Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements soldered or brazed or welded
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0063Three-dimensional shapes
    • A61F2230/0069Three-dimensional shapes cylindrical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0058Additional features; Implant or prostheses properties not otherwise provided for
    • A61F2250/0096Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0058Additional features; Implant or prostheses properties not otherwise provided for
    • A61F2250/0096Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers
    • A61F2250/0098Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers radio-opaque, e.g. radio-opaque markers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K2103/00Materials to be soldered, welded or cut
    • B23K2103/08Non-ferrous metals or alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K2103/00Materials to be soldered, welded or cut
    • B23K2103/18Dissimilar materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K2103/00Materials to be soldered, welded or cut
    • B23K2103/18Dissimilar materials
    • B23K2103/26Alloys of Nickel and Cobalt and Chromium
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49826Assembling or joining

Definitions

  • This invention relates to a method of making a machined and polished tubular metal prosthesis that defines a lumen around a long axis of the prosthesis and to which is welded a component of another metal that has opposed major surfaces that are arcuate luminal and abluminal surfaces relative to said long axis.
  • WO-A-02/15820 discloses a self-expanding stent of nickel titanium shape memory alloy that carries a ring of spoons of tantalum at each end of the tube of the stent, these tantalum spoons serving as radiopaque markers so that the stent prosthesis can be located by radiographic techniques, when inside the body of a patient.
  • polishing is conventionally accomplished by an electro-polishing procedure and, in electro-polishing, the rate of removal of solid material from the surface being polished will vary, according to the chemical composition of the surface and the chemical composition of the fluid medium in contact with that surface. For example, in the case of a NITINOL nickel titanium memory metal stent with tantalum radiopaque markers, electropolishing can remove NITINOL four times as fast as it removes tantalum.
  • the present inventors have recognised a problem with electro-polishing a prosthesis such as the one disclosed in the WO document because, for any given electrolyte, the rate of electro-polishing of the tantalum spoon is liable to be substantially different from the rate of polishing of the nickel titanium prosthesis material.
  • Polishing the tantalum spoon separate from the nickel titanium stent matrix would foe one way to manage the rate of removal of material from the surface being polished.
  • electro-polishing is always liable to introduce some uncertainty as to the precise dimensions of the polished workplace.
  • any electro-polishing prior to welding is liable to detract from the precision of placement of the respective components each side of the welding interface. Any such loss of precision can reduce the level of confidence in the integrity of the weld because, ideally, the gap between the components at the welding interface, to be filled by weld metal, should be precisely defined, and constant.
  • polishing covers any method of removing edges, surface roughness or imperfections. Electropolishing is one way. Chemical polishing, such as etching, is another. Mechanical polishing, such as tumbling or sand-blasting, is yet another.
  • a method of making a prosthesis as stated above is characterised by the steps of 1) polishing at least one of the component and the prosthesis; 2) providing the respective complementary edge portions as ramp surfaces which, prior to said welding, can approach each other as the component moves in one direction along the long axis relative to the prosthesis, and can move away from each other, vice versa, when the component is moved in the opposite sense along the axis; 3) moving the component and the prosthesis relative to each other along the said axis, to approximate the respective ramp surfaces ready for welding; and 4) welding together the approximated ramp surfaces.
  • a tubular metal prosthesis such as is made by the method above, is characterised in that the complementary respective edge portions are ramp surfaces which (in the absence of welding) can approach each other as the component moves in one direction along the long axis relative to the prosthesis, and move away from each other vice versa when the component is moved in the opposite sense along the axis; and the ramp surfaces of at lease one of the component and the prosthesis that receives the component exhibit polished surfaces.
  • the ramp surfaces compensate for any variability in the amount of material removed from the complementary edge portions during polishing prior to welding, in that relative axial movement of the ramp surfaces with respect to each other can compensate for more or less removal of material from the ramp surfaces during polishing. It may be that the relative axial positions of the prosthesis, and the component welded to it after welding vary to some extent but, in accordance with the invention, this is to be preferred over the situation where these relative axial positions are maintained constant, but at the cost of having a welding gap that varies according to the amount of material previously removed by polishing.
  • the tantalum spoons of the above-mentioned WO document have edge portions that complement corresponding edge portions on the nickel titanium stent, with the portions each side of the welding interface having a recognisable male/female relationship, and with the female portion being exhibited on the radiopaque tantalum marker spoons or other component to be welded to the prosthesis.
  • Such a male/female relationship is visualised for the ramp surfaces of the present invention. Indeed, it is envisaged that the male portion would exhibit an arrowhead shape with a tip at one end and a shank at the other and that the component with the female edge portions would exhibit at least one re-entrant portion for engaging behind the arrowhead of the male portion.
  • FIG. 1 is a perspective view of a single welding interface between part of a tubular metal prosthesis and a component of a different metal to be welded to that prosthesis;
  • FIGS. 2 to 5 show, respectively, plan views of four variations on the design concept visible in FIG. 1 ;
  • FIG. 6 shows part of a ring of male portions that extends around the circumference of a tubular metal prosthesis
  • FIG. 7 shows (at slightly higher magnification) part of a ring of corresponding components of another metal, with female portions destined to be welded to the respective projecting male portions shown in FIG. 6 .
  • a stent 10 similar to the one shown in WO-A-02/15820 has, at each end, a ring of nodes 12 between adjacent struts 14 , 15 of the strut matrix of the stent.
  • a shank 16 extends axially away from each node 12 and the stent matrix as such, as far as the root 18 of an arrowhead shape 20 that lies between symmetrical and complementary ramp surfaces 22 and 24 that converge to a tip 26 of the arrowhead 20 to define a male portion that is approximated with a female portion of a tantalum marker spoon 30 that has an abluminal major surface 32 and (not visible in FIG. 1 ) an opposed luminal major surface 34 which faces the long axis of the stent tube so that the thickness or the tantalum spoon 30 lies within an annulus centered on the long axis of the stent.
  • the female portion chat receives the arrowhead 20 is provided by opposed symmetrical complementary ramp surfaces 36 and 38 which converge to the root or base 40 of what can be seen as a V-shaped recess to receive the ramp surfaces 22 an 24 of the arrowhead 20 .
  • a cylindrical throughbore 42 At the base of the groove 40 there is a cylindrical throughbore 42 which is provided for reducing the risk of crack-initiation and propagation from the root of the V-shaped groove that receives the arrowhead 20 .
  • the stent matrix (typically made of nickel titanium shape memory alloy) is electro-polished before it is approximated with the tantalum spoon 30 .
  • the tantalum spoon 30 likely still part of a laser cut tube of tantalum and in the company of a plurality of other tantalum spoons that extends around the axis of the tubular workpiece (see the description in WO-A-02/15820) is also electro-polished and, after separate electro-polishing of the tantalum components and the nickel titanium components, the respective arrowhead male portions 20 can be brought into approximation with the corresponding female ramp surfaces of the respective tantalum spoons 30 , ready for welding.
  • FIG. 1 does reveal a small welding gap between ramp surfaces 22 and 36 , and surfaces 24 and 38 . This is the gap that is filled with weld metal in consequence of the welding step of assembly of the tantalum spoons 30 to the stent prosthesis 10 . If the amount of material removed from the respective ramp surfaces during respective electro-polishing is different form what was predicted, this need have no disturbing effect on the desired welding gap, provided that prior to welding there is a judicious relative axial movement of the male and female portions so as to bring about the desired optimal welding gap between the respective ramp surfaces.
  • FIG. 2 is provided with reference numbers corresponding to those of FIG. 1 and, we think, needs no further text description.
  • FIG. 3 differs only slightly from FIG. 2 , in that the female ramp surfaces do not run as far as the marginal edge of the tantalum component. Rather, the ramp surfaces are set back from the edge 50 , in that the ramp surface 36 continues as an unramped axially aligned edge 52 and, likewise, ramp surface 38 continues as an axially aligned straight edge 54 , parallel to edge 52 . Recessing the arrowhead “inside” the tantalum spoon avoids any adverse effects that might flow from having the acute angle between the arrowhead ramp surfaces 22 and 24 and the base 56 of the arrowhead lying outside the envelope of the tantalum spoon 30 .
  • the ramp surfaces are arcuate rather than straight, so the welding gap is not mathematically constant but nevertheless changes with relative axial movement of the ramp surfaces and, second, the arrowhead is gripped by re-entrant portions 60 that flank the shank 16 .
  • This engagement can be, as a matter of design preference, either resilient or of form-fit conception, with the arrowhead being introduced from radially inside or outside the female receiving portion in the component 30 .
  • FIG. 5 reveals a further variation, and difference from FIG. 4 , in that the arrowhead shape includes two terminal barbs 70 which can be resilient enough to locate the arrowhead with the cavity in the spoon 30 .
  • a ring of male projections 20 can be located around the circumference of the prosthesis, and offered up to a corresponding ring of recesses, each with root 40 , in respective components of another metal such as spoons 30 .
  • the ring of spoons can constitute a complete ring of material around the lumen of the prosthesis, with only laser cut gaps in between adjacent spoons.
  • each component can be found all within a common workpiece, from which they are parted after welding, as described above.
  • each component can be separate from the outset, then prepared individually, and then welded individually to the prosthesis.
  • the prosthesis needs to be polished to a high level and, generally speaking, the excellence and integrity of the polishing of the prosthesis overall should, if anything, be higher than the level of polishing of a radiopaque marker on the prosthesis.
  • the ramp surfaces that characterise the present invention can compensate for variations, prior to welding, in the weld surfaces of the prosthesis and component, respectively.

Abstract

For welding a polished component of one metal to a polished prosthesis of another metal, ramp surfaces are used, to compensate for loss of precise dimensions of the two components at the surfaces that face each other at the weld interface, during the respective polishing procedures for the two metals.

Description

    TECHNICAL FIELD
  • This invention relates to a method of making a machined and polished tubular metal prosthesis that defines a lumen around a long axis of the prosthesis and to which is welded a component of another metal that has opposed major surfaces that are arcuate luminal and abluminal surfaces relative to said long axis.
  • BACKGROUND PRIOR ART
  • One disclosure of such a prosthesis is to be found in WO-A-02/15820 of the present applicant. The WO document discloses a self-expanding stent of nickel titanium shape memory alloy that carries a ring of spoons of tantalum at each end of the tube of the stent, these tantalum spoons serving as radiopaque markers so that the stent prosthesis can be located by radiographic techniques, when inside the body of a patient.
  • It is customary to polish a prosthesis during manufacture, prior to implantation in the body, for the obvious reason that, at the moment of implantation, there should be no surfaces in a condition of anything less than full integrity. Polishing is conventionally accomplished by an electro-polishing procedure and, in electro-polishing, the rate of removal of solid material from the surface being polished will vary, according to the chemical composition of the surface and the chemical composition of the fluid medium in contact with that surface. For example, in the case of a NITINOL nickel titanium memory metal stent with tantalum radiopaque markers, electropolishing can remove NITINOL four times as fast as it removes tantalum. Indeed, the present inventors have recognised a problem with electro-polishing a prosthesis such as the one disclosed in the WO document because, for any given electrolyte, the rate of electro-polishing of the tantalum spoon is liable to be substantially different from the rate of polishing of the nickel titanium prosthesis material.
  • Polishing the tantalum spoon separate from the nickel titanium stent matrix would foe one way to manage the rate of removal of material from the surface being polished. However, electro-polishing is always liable to introduce some uncertainty as to the precise dimensions of the polished workplace. Thus, when two components of a workpiece are to be approximated precisely, and then welded together, any electro-polishing prior to welding is liable to detract from the precision of placement of the respective components each side of the welding interface. Any such loss of precision can reduce the level of confidence in the integrity of the weld because, ideally, the gap between the components at the welding interface, to be filled by weld metal, should be precisely defined, and constant.
  • How, then, is one to reconcile integrity of the welded joint with precision polishing of the components of different metals? This is the problem that the present inventors addressed, and the present invention represents a solution to that problem.
  • In this specification, the word “polishing” covers any method of removing edges, surface roughness or imperfections. Electropolishing is one way. Chemical polishing, such as etching, is another. Mechanical polishing, such as tumbling or sand-blasting, is yet another.
  • SUMMARY OF THE INVENTION
  • In accordance with one aspect of the present invention, a method of making a prosthesis as stated above is characterised by the steps of 1) polishing at least one of the component and the prosthesis; 2) providing the respective complementary edge portions as ramp surfaces which, prior to said welding, can approach each other as the component moves in one direction along the long axis relative to the prosthesis, and can move away from each other, vice versa, when the component is moved in the opposite sense along the axis; 3) moving the component and the prosthesis relative to each other along the said axis, to approximate the respective ramp surfaces ready for welding; and 4) welding together the approximated ramp surfaces.
  • In another aspect of the present invention, a tubular metal prosthesis, such as is made by the method above, is characterised in that the complementary respective edge portions are ramp surfaces which (in the absence of welding) can approach each other as the component moves in one direction along the long axis relative to the prosthesis, and move away from each other vice versa when the component is moved in the opposite sense along the axis; and the ramp surfaces of at lease one of the component and the prosthesis that receives the component exhibit polished surfaces.
  • It will appreciated that the ramp surfaces compensate for any variability in the amount of material removed from the complementary edge portions during polishing prior to welding, in that relative axial movement of the ramp surfaces with respect to each other can compensate for more or less removal of material from the ramp surfaces during polishing. It may be that the relative axial positions of the prosthesis, and the component welded to it after welding vary to some extent but, in accordance with the invention, this is to be preferred over the situation where these relative axial positions are maintained constant, but at the cost of having a welding gap that varies according to the amount of material previously removed by polishing.
  • The reader will appreciate that some sort of tool or jig or clamp will be required, in order to support the prosthesis and component in approximated positions where the desired welding gap is presented for receipt of weld metal. The construction of any such tool, jig or clamp, is a matter for the skilled reader. Whereas optimal automated production of a stream of stents might require construction of a special tool, a more labour-intensive or custom-welding procedure would present no difficulties for a stent manufacturer.
  • It is routine and conventional these days to machine a metal prosthesis from a tube of raw material. One way is by etching procedures, for example, when the tube is of stainless steel. However, laser cutting of a stent matrix in the cylindrical wall of the tubular workpiece is by now an intensively used and well-understood method for making a metal prosthesis such as a self-expanding stent out of a tubular raw material such as nickel titanium shape memory alloy (NITINOL trade mark). For the skilled stent manufacturer, therefore, it is not a matter of difficulty to program the laser cutter to provide ramp surfaces in complementary edge portions of a tubular metal prosthesis and a component to be welded to that prosthesis.
  • The tantalum spoons of the above-mentioned WO document have edge portions that complement corresponding edge portions on the nickel titanium stent, with the portions each side of the welding interface having a recognisable male/female relationship, and with the female portion being exhibited on the radiopaque tantalum marker spoons or other component to be welded to the prosthesis. Such a male/female relationship is visualised for the ramp surfaces of the present invention. Indeed, it is envisaged that the male portion would exhibit an arrowhead shape with a tip at one end and a shank at the other and that the component with the female edge portions would exhibit at least one re-entrant portion for engaging behind the arrowhead of the male portion.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • For a better understanding of the present invention, and to show how the same may be carried into effect, reference will now be made, be way of example, to the accompanying drawings, in which
  • FIG. 1 is a perspective view of a single welding interface between part of a tubular metal prosthesis and a component of a different metal to be welded to that prosthesis;
  • FIGS. 2 to 5 show, respectively, plan views of four variations on the design concept visible in FIG. 1;
  • FIG. 6 shows part of a ring of male portions that extends around the circumference of a tubular metal prosthesis; and
  • FIG. 7 shows (at slightly higher magnification) part of a ring of corresponding components of another metal, with female portions destined to be welded to the respective projecting male portions shown in FIG. 6.
  • DETAILED DESCRIPTION
  • Referring to FIG. 1, a stent 10 similar to the one shown in WO-A-02/15820 has, at each end, a ring of nodes 12 between adjacent struts 14, 15 of the strut matrix of the stent. A shank 16 extends axially away from each node 12 and the stent matrix as such, as far as the root 18 of an arrowhead shape 20 that lies between symmetrical and complementary ramp surfaces 22 and 24 that converge to a tip 26 of the arrowhead 20 to define a male portion that is approximated with a female portion of a tantalum marker spoon 30 that has an abluminal major surface 32 and (not visible in FIG. 1) an opposed luminal major surface 34 which faces the long axis of the stent tube so that the thickness or the tantalum spoon 30 lies within an annulus centered on the long axis of the stent.
  • The female portion chat receives the arrowhead 20 is provided by opposed symmetrical complementary ramp surfaces 36 and 38 which converge to the root or base 40 of what can be seen as a V-shaped recess to receive the ramp surfaces 22 an 24 of the arrowhead 20. At the base of the groove 40 there is a cylindrical throughbore 42 which is provided for reducing the risk of crack-initiation and propagation from the root of the V-shaped groove that receives the arrowhead 20.
  • In manufacture, the stent matrix (typically made of nickel titanium shape memory alloy) is electro-polished before it is approximated with the tantalum spoon 30. Likewise, the tantalum spoon 30, likely still part of a laser cut tube of tantalum and in the company of a plurality of other tantalum spoons that extends around the axis of the tubular workpiece (see the description in WO-A-02/15820) is also electro-polished and, after separate electro-polishing of the tantalum components and the nickel titanium components, the respective arrowhead male portions 20 can be brought into approximation with the corresponding female ramp surfaces of the respective tantalum spoons 30, ready for welding.
  • FIG. 1 does reveal a small welding gap between ramp surfaces 22 and 36, and surfaces 24 and 38. This is the gap that is filled with weld metal in consequence of the welding step of assembly of the tantalum spoons 30 to the stent prosthesis 10. If the amount of material removed from the respective ramp surfaces during respective electro-polishing is different form what was predicted, this need have no disturbing effect on the desired welding gap, provided that prior to welding there is a judicious relative axial movement of the male and female portions so as to bring about the desired optimal welding gap between the respective ramp surfaces.
  • Turning now to the remaining drawing figures, FIG. 2 is provided with reference numbers corresponding to those of FIG. 1 and, we think, needs no further text description. FIG. 3 differs only slightly from FIG. 2, in that the female ramp surfaces do not run as far as the marginal edge of the tantalum component. Rather, the ramp surfaces are set back from the edge 50, in that the ramp surface 36 continues as an unramped axially aligned edge 52 and, likewise, ramp surface 38 continues as an axially aligned straight edge 54, parallel to edge 52. Recessing the arrowhead “inside” the tantalum spoon avoids any adverse effects that might flow from having the acute angle between the arrowhead ramp surfaces 22 and 24 and the base 56 of the arrowhead lying outside the envelope of the tantalum spoon 30.
  • Turning to FIG. 4, there is shown, two further variations. First, the ramp surfaces are arcuate rather than straight, so the welding gap is not mathematically constant but nevertheless changes with relative axial movement of the ramp surfaces and, second, the arrowhead is gripped by re-entrant portions 60 that flank the shank 16. This engagement can be, as a matter of design preference, either resilient or of form-fit conception, with the arrowhead being introduced from radially inside or outside the female receiving portion in the component 30.
  • FIG. 5 reveals a further variation, and difference from FIG. 4, in that the arrowhead shape includes two terminal barbs 70 which can be resilient enough to locate the arrowhead with the cavity in the spoon 30. From FIGS. 6 and 7 it will be appreciated that a ring of male projections 20 can be located around the circumference of the prosthesis, and offered up to a corresponding ring of recesses, each with root 40, in respective components of another metal such as spoons 30. Just as in WO 02/15820 mentioned above, the ring of spoons can constitute a complete ring of material around the lumen of the prosthesis, with only laser cut gaps in between adjacent spoons.
  • In the case of welding a plurality of components (such as radiopaque markers) to a prosthesis, the components can be found all within a common workpiece, from which they are parted after welding, as described above. Alternatively, each component can be separate from the outset, then prepared individually, and then welded individually to the prosthesis.
  • It will be appreciated that the prosthesis needs to be polished to a high level and, generally speaking, the excellence and integrity of the polishing of the prosthesis overall should, if anything, be higher than the level of polishing of a radiopaque marker on the prosthesis.
  • The ramp surfaces that characterise the present invention can compensate for variations, prior to welding, in the weld surfaces of the prosthesis and component, respectively.

Claims (19)

1. A tubular metal stent, comprising:
a stent body formed from a first material including:
a first stent ring including struts connected by nodes positioned at a first end of the stent body,
a plurality of shanks extending axially away from nodes on the first stent ring along a longitudinal axis of the stent body,
each of the plurality of shanks having a head portion,
each head portion including first and second polished ramp surfaces converging and meeting at a point axially away from the stent body; and
a plurality of radiopaque markers formed from a second material different from the first material, each of the markers including an end recess having complementary polished third and fourth ramp surfaces that abut the polished first and second ramp surfaces when the head portion is inserted into the end recess.
2. The stent according to claim 1 wherein the end recess of each of the radiopaque markers includes axially aligned edges parallel to the longitudinal axis of the stent body adjacent the polished third and fourth ramp surfaces.
3. The stent according to claim 2 further comprising a second stent ring including struts connected by nodes positioned at a second end of the stent body opposite the first end of the stent body.
4. The stent according to claim 3 further comprising a plurality of shanks extending axially away from nodes on the second stent ring along a longitudinal axis of the stent body, each of the plurality of shanks having a head portion.
5. The stent according to claim 4 wherein each head portion includes first and second polished ramp surfaces converging and meeting at a point axially away from the stent body.
6. The stent according to claim 1 wherein the head portion polished first and second ramp surfaces and end recess complementary polished third and fourth ramp surfaces have an arcuate shape.
7. The stent according to claim 6 further comprising a second stent ring including struts connected by nodes positioned at a second end of the stent body opposite the first end of the stent body.
8. The stent according to claim 7 further comprising a plurality of shanks extending axially away from nodes on the second stent ring along a longitudinal axis of the stent body, each of the plurality of shanks having a head portion.
9. The stent according to claim 8 wherein each head portion includes first and second polished ramp surfaces converging and meeting at a point axially away from the stent body.
10. A tubular metal stent, comprising:
a stent body formed from a first material including:
a first stent ring including struts connected by nodes positioned at a first end of the stent body,
a plurality of shanks extending axially away from nodes on the first stent ring along a longitudinal axis of the stent body,
each of the plurality of shanks having a head portion,
each head portion including first and second polished ramp surfaces converging and meeting at a point axially away from the stent body; and
a plurality of radiopaque markers formed from a second material different from the first material, each of the markers including an end recess having complementary polished third and fourth ramp surfaces that abut the polished first and second ramp surfaces when the head portion is inserted into the end recess
wherein the head portion polished first and second ramp surfaces and end recess complementary polished third and fourth ramp surfaces have an arcuate shape
11. The stent according to claim 10 further comprising a second stent ring including struts connected by nodes positioned at a second end of the stent body opposite the first end of the stent body.
12. The stent according to claim 11 further comprising a plurality of shanks extending axially away from nodes on the second stent ring along a longitudinal axis of the stent body, each of the plurality of shanks having a head portion.
13. The stent according to claim 12 wherein each head portion includes first and second polished ramp surfaces converging and meeting at a point axially away from the stent body.
14. The stent according to claim 13 wherein each of the radiopaque markers further comprises a cylindrical throughbore at an end of the recess.
15. A tubular metal stent, comprising:
a stent body formed from a first material, including:
a first stent ring including struts connected by nodes positioned at a first end of the stent body,
a plurality of shanks extending axially away from nodes on the first stent ring along a longitudinal axis of the stent body,
an arrow-shaped head extending from each of the plurality of shanks,
each arrow-shaped head portion including first and second polished ramp surfaces; and
a plurality of radiopaque markers formed from a second material different from the first material, each of the markers including an end recess having complementary polished third and fourth ramp surfaces that abut the polished first and second ramp surfaces when the head portion is inserted into the end recess.
16. The stent according to claim 15 further comprising a second stent ring including struts connected by nodes positioned at a second end of the stent body opposite the first end of the stent body.
17. The stent according to claim 16 further comprising a plurality of shanks extending axially away from nodes on the second stent ring along a longitudinal axis of the stent body, each of the plurality of shanks having a head portion.
18. The stent according to claim 17 wherein each head portion includes first and second polished ramp surfaces converging and meeting at a point axially away from the stent body.
19. The stent according to claim 18 wherein each of the radiopaque markers further comprises a cylindrical throughbore at an end of the recess.
US15/269,866 2006-07-10 2016-09-19 Tubular Metal Prosthesis and Method of Making It Abandoned US20170007429A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/269,866 US20170007429A1 (en) 2006-07-10 2016-09-19 Tubular Metal Prosthesis and Method of Making It

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB0616370.9 2006-07-10
GBGB0613670.9A GB0613670D0 (en) 2006-07-10 2006-07-10 Tubular metal prosthesis and method of making it
US12/373,116 US9445924B2 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it
PCT/EP2007/057041 WO2008006830A1 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it
US15/269,866 US20170007429A1 (en) 2006-07-10 2016-09-19 Tubular Metal Prosthesis and Method of Making It

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/EP2007/057041 Continuation WO2008006830A1 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it
US12/373,116 Continuation US9445924B2 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it

Publications (1)

Publication Number Publication Date
US20170007429A1 true US20170007429A1 (en) 2017-01-12

Family

ID=36926757

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/373,116 Active 2030-10-02 US9445924B2 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it
US15/269,866 Abandoned US20170007429A1 (en) 2006-07-10 2016-09-19 Tubular Metal Prosthesis and Method of Making It

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/373,116 Active 2030-10-02 US9445924B2 (en) 2006-07-10 2007-07-10 Tubular metal prosthesis and method of making it

Country Status (4)

Country Link
US (2) US9445924B2 (en)
EP (1) EP2040641B1 (en)
GB (1) GB0613670D0 (en)
WO (1) WO2008006830A1 (en)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0020491D0 (en) 2000-08-18 2000-10-11 Angiomed Ag Stent with attached element and method of making such a stent
GB0609841D0 (en) 2006-05-17 2006-06-28 Angiomed Ag Bend-capable tubular prosthesis
GB0609911D0 (en) 2006-05-18 2006-06-28 Angiomed Ag Bend-capable stent prosthesis
GB0616729D0 (en) 2006-08-23 2006-10-04 Angiomed Ag Method of welding a component to a shape memory alloy workpiece
GB0616999D0 (en) 2006-08-29 2006-10-04 Angiomed Ag Annular mesh
WO2008028964A2 (en) 2006-09-07 2008-03-13 Angiomed Gmbh & Co. Medizintechnik Kg Helical implant having different ends
GB0622465D0 (en) 2006-11-10 2006-12-20 Angiomed Ag Stent
GB0624419D0 (en) 2006-12-06 2007-01-17 Angiomed Ag Stenting ring with marker
GB0703379D0 (en) 2007-02-21 2007-03-28 Angiomed Ag Stent with radiopaque marker
GB0706499D0 (en) 2007-04-03 2007-05-09 Angiomed Ag Bendable stent
GB0717481D0 (en) 2007-09-07 2007-10-17 Angiomed Ag Self-expansible stent with radiopaque markers
AU2013336672B2 (en) * 2012-10-25 2017-11-23 Sahajanand Medical Technologies Private Limited Radiopaque marker for bioresorbable stents
DE102015117666B4 (en) * 2015-10-16 2019-03-28 Acandis Gmbh Endovascular medical device, treatment system with such a device and manufacturing method
US11622872B2 (en) 2016-05-16 2023-04-11 Elixir Medical Corporation Uncaging stent
EP3457985B1 (en) 2016-05-16 2021-02-17 Elixir Medical Corporation Uncaging stent

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020120323A1 (en) * 2001-02-26 2002-08-29 Intratherapeutics, Inc. Implant delivery system with interlock
US20040015228A1 (en) * 2000-08-17 2004-01-22 Sylvie Lombardi Implant with attached element and method of making such an implant
US20050060025A1 (en) * 2003-09-12 2005-03-17 Mackiewicz David A. Radiopaque markers for medical devices
US20140014530A1 (en) * 2012-07-13 2014-01-16 Abbott Cardiovascular Systems, Inc. Methods for passivating metallic implantable medical devices including radiopaque markers

Family Cites Families (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB453944A (en) 1935-04-10 1936-09-22 John Walter Anderson Improvements in couplings for vehicles
FR2626046A1 (en) 1988-01-18 1989-07-21 Caoutchouc Manuf Plastique Device for joining panels or for producing conduits and its applications
DE4130431A1 (en) 1991-09-13 1993-03-18 Liselotte Dr Sachse Plastics urethral prosthesis - consists of tube and reinforced with metal rings placed in tube mould or fitted within plastics layers of tube
EP0662806B1 (en) 1993-07-23 2001-04-11 Cook Incorporated A flexible stent having a pattern formed from a sheet of material
JPH07315147A (en) 1994-05-23 1995-12-05 Nishikawa Rubber Co Ltd Attachment structure for drip weather strip
IL115755A0 (en) 1994-10-27 1996-01-19 Medinol Ltd X-ray visible stent
CA2163824C (en) 1994-11-28 2000-06-20 Richard J. Saunders Method and apparatus for direct laser cutting of metal stents
US6334871B1 (en) 1996-03-13 2002-01-01 Medtronic, Inc. Radiopaque stent markers
DE19614160A1 (en) 1996-04-10 1997-10-16 Variomed Ag Stent for transluminal implantation in hollow organs
US5855596A (en) 1996-06-25 1999-01-05 International Business Machines Corporation Modular wire band stent
DE29621207U1 (en) 1996-12-06 1997-01-30 Roland Man Druckmasch Fastening a heat sink on a printed circuit board
DE19653720A1 (en) 1996-12-10 1998-06-18 Biotronik Mess & Therapieg Stent
US5868783A (en) 1997-04-16 1999-02-09 Numed, Inc. Intravascular stent with limited axial shrinkage
US5741327A (en) 1997-05-06 1998-04-21 Global Therapeutics, Inc. Surgical stent featuring radiopaque markers
DE19728337A1 (en) 1997-07-03 1999-01-07 Inst Mikrotechnik Mainz Gmbh Implantable stent
ES2290995T3 (en) 1997-09-24 2008-02-16 Med Institute, Inc. RADIALLY EXPANDABLE ENDOPROTESIS.
US6022374A (en) 1997-12-16 2000-02-08 Cardiovasc, Inc. Expandable stent having radiopaque marker and method
US6503271B2 (en) 1998-01-09 2003-01-07 Cordis Corporation Intravascular device with improved radiopacity
DE29904817U1 (en) 1999-03-16 1999-05-27 Amg Handelsgesellschaft Fuer A Blood vessel support device
US6464723B1 (en) 1999-04-22 2002-10-15 Advanced Cardiovascular Systems, Inc. Radiopaque stents
US6379381B1 (en) 1999-09-03 2002-04-30 Advanced Cardiovascular Systems, Inc. Porous prosthesis and a method of depositing substances into the pores
US6471721B1 (en) 1999-12-30 2002-10-29 Advanced Cardiovascular Systems, Inc. Vascular stent having increased radiopacity and method for making same
GB0003387D0 (en) * 2000-02-14 2000-04-05 Angiomed Ag Stent matrix
DE10026307A1 (en) 2000-05-26 2001-11-29 Variomed Ag Balzers Stent, positioning element and insertion catheter
US6540777B2 (en) 2001-02-15 2003-04-01 Scimed Life Systems, Inc. Locking stent
US8197535B2 (en) 2001-06-19 2012-06-12 Cordis Corporation Low profile improved radiopacity intraluminal medical device
DE10201151B4 (en) 2002-01-15 2007-10-04 Qualimed Innovative Medizinprodukte Gmbh Stent with marker
US20030225448A1 (en) 2002-05-28 2003-12-04 Scimed Life Systems, Inc. Polar radiopaque marker for stent
US20040015229A1 (en) 2002-07-22 2004-01-22 Syntheon, Llc Vascular stent with radiopaque markers
US7331986B2 (en) 2002-10-09 2008-02-19 Boston Scientific Scimed, Inc. Intraluminal medical device having improved visibility
EA010169B1 (en) 2002-12-17 2008-06-30 Флуор Корпорейшн Configurations and methods for acid gas and contaminant removal with near zero emission
US20040236409A1 (en) 2003-05-20 2004-11-25 Pelton Alan R. Radiopacity intraluminal medical device
ES2364555T3 (en) 2003-05-23 2011-09-06 Boston Scientific Limited CANNULAS WITH INCORPORATED LOOP TERMINATIONS.
US20040254637A1 (en) 2003-06-16 2004-12-16 Endotex Interventional Systems, Inc. Sleeve stent marker
US7854756B2 (en) 2004-01-22 2010-12-21 Boston Scientific Scimed, Inc. Medical devices
US7572289B2 (en) * 2004-01-27 2009-08-11 Med Institute, Inc. Anchoring barb for attachment to a medical prosthesis
US7243408B2 (en) 2004-02-09 2007-07-17 Boston Scientific Scimed, Inc. Process method for attaching radio opaque markers to shape memory stent
US20060216431A1 (en) * 2005-03-28 2006-09-28 Kerrigan Cameron K Electrostatic abluminal coating of a stent crimped on a balloon catheter
GB0616729D0 (en) 2006-08-23 2006-10-04 Angiomed Ag Method of welding a component to a shape memory alloy workpiece
GB0624419D0 (en) 2006-12-06 2007-01-17 Angiomed Ag Stenting ring with marker
GB0703379D0 (en) 2007-02-21 2007-03-28 Angiomed Ag Stent with radiopaque marker

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040015228A1 (en) * 2000-08-17 2004-01-22 Sylvie Lombardi Implant with attached element and method of making such an implant
US20020120323A1 (en) * 2001-02-26 2002-08-29 Intratherapeutics, Inc. Implant delivery system with interlock
US20050060025A1 (en) * 2003-09-12 2005-03-17 Mackiewicz David A. Radiopaque markers for medical devices
US20140014530A1 (en) * 2012-07-13 2014-01-16 Abbott Cardiovascular Systems, Inc. Methods for passivating metallic implantable medical devices including radiopaque markers

Also Published As

Publication number Publication date
EP2040641A1 (en) 2009-04-01
WO2008006830A1 (en) 2008-01-17
US9445924B2 (en) 2016-09-20
GB0613670D0 (en) 2006-08-16
EP2040641B1 (en) 2014-08-27
US20100070018A1 (en) 2010-03-18

Similar Documents

Publication Publication Date Title
US20170007429A1 (en) Tubular Metal Prosthesis and Method of Making It
JP5530357B2 (en) Self-expanding stent with radiopaque marker and method for manufacturing the same
US10213327B2 (en) Implant with attached element and method of making such an implant
JP4131750B2 (en) Artificial joints, especially hip joints
EP2112913B1 (en) Stent with radiopaque marker
EP2054190B1 (en) Method of welding a component to a shape memory alloy workpiece with provision of an extra cut for compensating the variations of dimension of workpiece and component
US11259918B2 (en) Frame for an implantable medical device and a method of manufacturing a frame for an implantable medical device
EP2088970B1 (en) Stenting ring with marker
US20040060161A1 (en) Methods of forming a heart valve stent
WO2005115276A1 (en) Stent with protective pads or bulges
CH672060A5 (en)
EP3257469B1 (en) Method for producing a dental prosthesis implant pillar by additive manufacturing and spark machining and facility for implementing such a method
EP3184075B1 (en) Method for producing an abutment and an associated dental prosthesis and dental prosthesis obtained by such a method
CN117425451A (en) Implant detachment mechanism
MXPA98008674A (en) Artificial articulation, in particular an artificial articulation for cad

Legal Events

Date Code Title Description
STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

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