Welded radially expandable endoprosthesis and the like

• US 5,304,200 A
• Filed: 01/13/1993
• Issued: 04/19/1994
• Est. Priority Date: 05/29/1991
• Status: Expired due to Term

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Spaulding, Ronald N.
• Primary Examiner(s): Rosenbaum, C. Fred
• Assistant Examiner(s): Bockelman, Mark
• Application Number:
  US08/004,179
• Time in Patent Office: 461 Days
• Field of Search: 604/8, 604/104, 604/281-282, 604/96-103, 606/108, 606/192-194, 606/198, 606/195, 623/1, 623/11-12, 623/901
• US Class Current: 623/1.16
• CPC Class Codes: A61F 2/88 the wire-like elements formed as helical or spiral coils forming a net-like or mesh-like structure A61F2/90
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: Y10S 623/901 Method of manufacturing prosthetic device

Abstract

Radially expandable endoprostheses or stents are provided, as well as their method of manufacture. These stents include a plurality of adjacent generally circumferential sections that are substantially axially positioned with respect to each other. Included are generally circumferentially disposed expandable segments that impart circumferential and radial expandability to the stents. The terminal portions of the end circumferential sections are welded directly to a portion of a generally adjacent circumferential section, and the welding preferably is carried out within an inert gas environment in a manner that minimizes crack formation at the weld locations.

Claims

1. A radially expandable endoprosthesis, comprising:

a plurality of generally circumferential sections, including end and intermediate generally circumferential sections, said end and intermediate generally circumferential sections being substantially adjacent to one another and generally parallel to each other in order to thereby substantially define an endoprosthesis having a longitudinal axis along which each of said generally circumferential sections are substantially axially spaced;

each of said generally circumferential sections includes an expandable segment that imparts radial expandability to said generally circumferential section whereby said section has an unexpanded insertion circumference and an expanded implantation circumference which is greater than said unexpanded insertion circumference;

said expandable segment of each generally circumferential section is a member that is bendable between a generally closed orientation and a generally opened orientation so as to impart radial expandability to the generally circumferential section;

said generally circumferential sections form a continuous helix-like structure that defines an axially extending endoprosthesis, the helix-like structure having terminal portions of said end sections;

each of said terminal portions of the end sections is welded to an adjacent one of said intermediate sections, thereby avoiding presentation of loose ends on the endoprosthesis, each of said welds directly securing the terminal portion to a bendable portion of the adjacent intermediate section, each of said welds has a generally tapering configuration having a feathered edge structure; and

each said weld is a laser-formed weld made while the endoprosthesis is encased within an enclosed welding compartment filled with an inert gas and substantially free of oxygen, the laser-formed weld having been formed by directing a laser beam through a wall of the enclosed welding compartment, which wall retains inert gas within the enclosed welding compartment and permits the laser beam to pass therethrough to form the laser-formed weld;

whereby the weld of the endoprosthesis exhibits substantial reduction of embrittlement and cracking, and the weld has significantly greater tensile strength, all when compared with an otherwise identical weld formed under a steam of the same inert gas and without the endoprosthesis being in the enclosed welding compartment.

2. The endoprosthesis according to claim 1, wherein said weld is a butt weld by which the terminal portion is generally perpendicular to the portion of the adjacent generally circumferential section to which it is welded.

3. The endoprosthesis according to claim 1, wherein said weld is a parallel weld by which the terminal portion is generally parallel to and closely engages the portion of the adjacent generally circumferential section to which it is welded.

4. The endoprosthesis according to claim 1, wherein said endoprosthesis is made of tantalum wire.

5. A method for making a radially expandable endoprosthesis, comprising the steps of:

winding an elongated strand around a narrow wrapping surface of a mandrel so as to form a wound stand having a plurality of turns therein;

subjecting the wound strand to flattening forces in order to form a generally flat undulating strand length;

generally helically wrapping the undulating strand length around a mandrel in order to provide a plurality of generally circumferential sections forming a continuous helix-like structure having a plurality of generally circumferential sections including end and intermediate generally circumferential sections;

welding a terminal portion of one of the generally circumferential end sections to an adjacent one of the intermediate generally circumferential sections, the welding step directly securing the terminal portion to the adjacent section to form a weld of generally tapering configuration having a feathered edge structure;

carrying out the welding step within an environment of inert gas, and the welding step includes encasing the endoprosthesis within an enclosed welding compartment substantially free of oxygen and filled with an inert gas; and

said welding step further includes directing a laser beam through a wall of the enclosed welding compartment, which wall retains inert gas within the welding compartment and permits the laser beam to pass therethrough, and to the area being welded to form a weld that exhibits substantial reduction of embrittlement and cracking and that has significantly greater tensile strength when compared with an otherwise identical weld formed under a stream of the same inert gas and without the endoprosthesis being in the enclosed welding compartment.

6. The method according to claim 5, wherein the inert gas atmosphere is argon gas.

7. The method according to claim 5, wherein the welding step includes providing a tail portion of the terminal portion which is present prior to welding and which does not remain as a tail portion upon completion of the welding step.

8. The method according to claim 5, wherein said winding step includes winding tantalum as the elongated strand, and said inert gas of the welding step is argon gas.

9. A radially expandable endoprosthesis made in accordance with a process comprising the steps of:

winding an elongated strand around a narrow wrapping surface of a mandrel so as to form a wound strand having a plurality of turns therein;

subjecting the wound strand to flattening forces in order to form a generally flat undulating strand length;

generally helically wrapping the undulating strand length around a mandrel in order to provide a plurality of generally circumferential sections forming a continuous helixlike structure having a plurality of generally circumferential sections including end and intermediate generally circumferential sections;

welding a terminal portion of one of the generally circumferential end sections to an adjacent one of the intermediate generally circumferential sections, the welding step directly securing terminal portion to the adjacent section to form a weld of generally tapering configuration having a feathered edge structure;

carrying out the welding step within an environment of inert gas, and the welding step includes encasing the endoprosthesis within an enclosed welding compartment substantially free of oxygen and filled with an inert gas; and

said welding step further includes directing a laser beam through a wall of the enclosed welding compartment, which wall retains inert gas within the welding compartment and permits the laser beam to pass therethrough and to the area being welded to form the weld;

whereby the weld of the endoprosthesis exhibits substantial reduction of embrittlement and cracking, and the weld has significantly greater tensile strength, all when compared with an otherwise identical weld formed under a stream of the same inert gas and without the endoprosthesis being in the enclosed welding compartment.

10. The endoprosthesis according to claim 9, wherein said winding step includes winding tantalum as the elongated strand.

11. The endoprosthesis according to claim 9, wherein the inert gas atmosphere is substantially argon gas and is free of oxygen.

12. The endoprosthesis according to claim 9, wherein the welding step includes providing a tail portion of the terminal portion which is present prior to welding and which does not remain as a tail portion upon completion of the welding step.