IP Library Granted Patent US 7,070,616
Granted Patent B2
US 7,070,616 · App. 10/699,014 · Granted Jul 4, 2006

Implantable valvular prosthesis

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,070,616
App. No.
10/699,014
Granted
Jul 4, 2006
Kind
B2
Abstract

The present invention relates to a medical device, and in particular, to a stent-based valve. The valve includes a radially expandable structural frame including an anchor structure having a first and a second open end, a connecting member having a first and a second end, and a cantilever valve strut having a first and a second end. The first end of the connecting member is attached to the second end of the anchor structure. The first end of the cantilever valve strut is cooperatively associated with the second end of the connecting member. The prosthetic valve further includes a biocompatible membrane assembly having a substantially tubular configuration disposed longitudinally about at least a portion of the connecting member. The membrane assembly has a first end having a first diameter and a second end having a second diameter, wherein the first diameter is greater than the second diameter. The first end of the membrane assembly is attached along the second end of the cantilever valve strut.

Claims (28)

1. A prosthetic valve comprising:

a radially expandable structural frame defining a longitudinal axis, including an anchor structure having first and second open ends, a connecting member having first and second ends, the first end of the connecting member being attached to the second end of the anchor structure, and a cantilever valve strut having first and second ends, wherein the first end of the cantilever valve strut is shaped into a semi-circular loop configuration and is cooperatively associated with the second end of the connecting member; and

a biocompatible membrane assembly having a substantially tubular configuration disposed longitudinally about the structural frame, the membrane assembly including a first end having a first diameter and a second end having a second diameter, wherein the first diameter is greater than the second diameter, the first end of the membrane assembly being attached along the second end of the cantilever valve strut.

2. The prosthetic valve of claim 1 wherein the anchor structure is formed from a lattice of interconnected elements, and has a substantially cylindrical configuration.

3. The prosthetic valve of claim 1 wherein the structural frame comprises a material selected from the group consisting of stainless steel, tantalum, platinum alloys, niobium alloy, cobalt alloy, and nickel-titanium alloy.

4. The prosthetic valve of claim 1 wherein the structural frame comprises a polymer.

5. The prosthetic valve of claim 1 wherein the biocompatible membrane assembly is formed from a flexible membrane-like material.

6. The prosthetic valve of claim 5 wherein the membrane-like material is a biological material.

7. The prosthetic valve of claim 6 wherein the biological material is a vein.

8. The prosthetic valve of claim 5 wherein the membrane-like material is a synthetic material.

9. The prosthetic valve of claim 8 wherein the synthetic material is an elastomeric polymer.

10. The prosthetic valve of claim 8 wherein the synthetic material is a bioabsorbable material.

11. The prosthetic valve of claim 8 wherein the synthetic material further comprises a reinforcement fiber.

12. The prosthetic valve of claim 1 wherein at least a portion of the structural frame is coated with an agent.

13. The prosthetic valve of claim 12 wherein the agent coating contains a therapeutic agent.

14. The prosthetic valve of claim 12 wherein the agent coating contains a pharmaceutic agent.

15. The prosthetic valve of claim 12 wherein the agent coating comprises an agent-eluting layer.

16. The prosthetic valve of claim 1 wherein at least a portion of the membrane assembly is coated with an agent.

17. The prosthetic valve of claim 16 wherein the agent coating contains a therapeutic agent.

18. The prosthetic valve of claim 16 wherein the agent coating contains a pharmaceutic agent.

19. The prosthetic valve of claim 16 wherein the agent coating comprises an agent-eluting layer.

20. The prosthetic valve of claim 1 wherein at least a portion of the membrane assembly is impregnated with a therapeutic agent.

21. The prosthetic valve of claim 1 wherein at least a portion of the membrane assembly is impregnated with a pharmaceutic agent.

22. The prosthetic valve of claim 1 wherein the connecting member is a substantially straight member oriented in a direction substantially parallel to the longitudinal axis.

23. The prosthetic valve of claim 1 wherein the second end of the cantilever valve strut has a substantially straight shape and oriented in a direction substantially parallel to the longitudinal axis.

24. The prosthetic valve of claim 1 wherein the second end of the tubular biocompatible membrane has a closed end.

25. The prosthetic valve of claim 1 wherein the second end of the tubular biocompartible membrane moves from a substantially open to a substantially closed position by the cantilever valve strut.

26. The prosthetic valve of claim 1 wherein the structural frame further comprises a proximal collar attached to the second end of the connecting member and first end of the cantilever valve strut.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2025
From: CARDINAL HEALTH SWITZERLAND 515 GMBH; CARDINAL HEALTH 529, LLC; CORDIS CORPORATION; FLEXIBLE STENTING SOLUTIONS, INC
To: CORDIS US CORP
Reel/Frame 072987/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2017
From: CORDIS CORPORATION
To: CARDINAL HEALTH SWITZERLAND 515 GMBH
Reel/Frame 042126/0259 →