Medical device with tensionably attached remodelable material

• US 8,128,682 B2
• Filed: 05/11/2010
• Issued: 03/06/2012
• Est. Priority Date: 04/11/2005
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Case, Brian C., Flagle, Jacob A., Paul, Ram H. Jr., Chambers, Sean D.
• Primary Examiner(s): Sweet, Thomas J
• Assistant Examiner(s): Stewart, Jason-Dennis
• Application Number:
  US12/777,947
• Publication Number:
  US 20100280586A1
• Time in Patent Office: 665 Days
• Field of Search: 623/1.24, 623/1.13, 623/1.15
• US Class Current: 623/1.24
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2475 Venous valves
• CPC Class Codes: A61F 2/86 Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2210/0004 bioabsorbable
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/0071 spherical
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0031 made from both resorbable and non-resorbable prosthetic parts, e.g. adjacent parts
• CPC Class Codes: A61F 2250/0071 breakable or frangible

Abstract

Medical devices for implantation in a body vessel, and methods of using and making the same, are provided. A medical device includes a support frame having struts and a weakened frame portion, and a remodelable material tensionably attached to the support frame. The weakened frame portion has a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force. The remodelable material restricts expansion of the frame from a radially compressed configuration to a radially expanded configuration when the weakened frame portion is in the first configuration. The remodelable material can form one or more valve leaflets adapted to regulate fluid flow in a body vessel, such as a vein.

Claims

1. An implantable medical device, comprising:

a self-expandable support frame having radially compressed and radially expanded configurations, the support frame having a perimeter that defines a lumen and comprising first, second, and third struts positioned along the perimeter, and a weakened frame portion joining the first and second struts and having a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force; and

a remodelable material having first, second and third edges, the first edge attached to the first strut and extending along the first strut to the weakened frame portion, the second edge attached to the third strut, and the third edge extending between the first and second edges and across the lumen and comprising a free edge not attached to the support frame;

wherein the remodelable material is tensionably attached to the first and third struts such that the remodlable material restricts expansion of the support frame from the radially compressed configuration to the radially expanded configuration when the weakened frame portion is in the first configuration.

2. The implantable medical device of claim 1, wherein the weakened frame portion comprises a separate frame segment attached to the first and second struts.

3. The implantable medical device of claim 2, wherein the weakened frame portion comprises a curved frame segment attached to the first strut at a first dislocating joint and attached to the second strut at a second dislocating joint.

4. The implantable medical device of claim 3, wherein one of the first and second dislocating joints comprises a biodegradable adhesive joining the curved frame segment to the first or second strut.

5. The implantable medical device of claim 3, further comprising a flexible retaining ring encircling the one of the first and second dislocating joints.

6. The implantable medical device of claim 1, wherein the weakened frame portion comprises a strut comprising a non-bioabsorbable core material surrounded by a bioabsorbable material.

7. The implantable medical device of claim 1, wherein the weakened frame portion comprises a strut comprising a non-bioabsorbable core material having an outer surface defining a series of indentations and a rigid bioabsorbable material deposited in the indentations.

8. The implantable medical device of claim 1, wherein the support frame further comprises a fourth strut positioned along the perimeter and a second weakened frame portion joining the third and fourth struts;

the second edge of the bioremodelable material attached to the third strut and extending along the third strut to the second weakened frame portion.

9. The implantable medical device of claim 1, wherein the first and third struts are positioned opposite each other relative to the lumen of the support frame.

10. The implantable medical device of claim 1, wherein the support frame comprises stainless steel.

11. The implantable medical device of claim 1, wherein the support frame comprises a nickel titanium alloy.

12. The implantable medical device of claim 1, wherein the support frame comprises a cobalt-chromium alloy.

13. The implantable medical device of claim 1, wherein the remodelable material comprises a collagenous material.

14. The implantable medical device of claim 1, wherein the remodelable material comprises an extracellular matrix material.

15. The implantable medical device of claim 14, wherein the extracellular matrix material comprises one of submucosa, renal capsule membrane, dermal collagen, dura mater, pericardium, fascia lata, serosa, peritoneum and liver basement membrane.

16. The implantable medical device of claim 14, wherein the extracellular matrix material comprises submucosa selected from the group consisting of intestinal submucosa, stomach submucosa, urinary bladder submucosa, and uterine submucosa.

17. The implantable medical device of claim 14, wherein the extracellular matrix material comprises small intestine submucosa.

18. The implantable medical device of claim 14, further comprising a non-native bioactive component incorporated into the extracellular matrix material.

19. An implantable medical device, comprising:

a self-expandable support frame having radially compressed and radially expanded configurations, the support frame having a perimeter that defines a lumen and comprising first, second, third and fourth struts positioned along the perimeter, a first weakened frame portion positioned on the perimeter and joining the first and second struts, and a second weakened frame portion positioned on the perimeter and joining the third and fourth struts, the first weakened frame portion positioned opposite the second weakened frame portion with respect to the lumen; and

a remodelable material having first, second and third edges, the first edge attached to the first strut and extending along the first strut to the weakened frame portion, the second edge attached to the third strut and extending along the third strut to the second weakened frame portion, and the third edge extending between the first and second edges and across the lumen and comprising a free edge not attached to the support frame;

wherein the first and second weakened frame portions each have a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force; and

wherein the remodelable material is tensionably attached to the first and third struts such that the remodelable material restricts expansion of the support frame from the radially compressed configuration to the radially expanded configuration when the weakened frame portion is in the first configuration.

20. An implantable medical device, comprising:

a self-expandable support frame having radially compressed and radially expanded configurations, the support frame having a perimeter that defines a lumen and comprising first, second, third and fourth struts positioned along the perimeter, a first weakened frame portion positioned on the perimeter and joining the first and second struts, and a second weakened frame portion positioned on the perimeter and joining the third and fourth struts, the first weakened frame portion positioned opposite the second weakened frame portion with respect to the lumen; and

a remodelable material having first, second and third edges, the first edge attached to the first strut and extending along the first strut to the weakened frame portion, the second edge attached to the third strut and extending along the third strut to the second weakened frame portion, and the third edge extending between the first and second edges and across the lumen and comprising a free edge not attached to the support frame;

wherein the first and second weakened frame portions each have a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force;

wherein the first weakened frame portion comprises a first curved frame segment attached to the first strut at a first dislocating joint and attached to the second strut at a second dislocating joint and the second weakened frame portion comprises a second curved frame segment attached to the third strut at a third dislocating joint and attached to the fourth strut at a fourth dislocating joint; and

wherein the remodelable material is tensionably attached to the first and third struts such that the remodelable material restricts expansion of the support frame from the radially compressed configuration to the radially expanded configuration when the weakened frame portion is in the first configuration.