# US 9,867,727 B2 · Endovascular graft

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- Number: US 9,867,727 B2
- Document ID: US9867727B2
- Status: Granted
- Kind: B2
- Application number: 14/320,773
- Filed: 2014-07-01
- Published: 2014-10-23
- Granted: 2018-01-16
- Earliest claimed: 1998-02-09
- Assignees: TriVascular, Inc.
- Applicants: TriVascular, Inc.
- Inventors: Michael V. Chobotov
- Web page: https://patentgrep.com/patent/US9867727B2

## CPC

- A61F 2/958: Inflatable balloons for placing stents or stent-grafts
- A61F 2/06: Blood vessels
- A61F 2/07: Stent-grafts
- A61F 2/90: characterised by a net-like or mesh-like structure
- A61F 2/915: with bands having a meander structure, adjacent bands being connected to each other
- A61F 2/945: hardenable, e.g. stents formed in situ
- A61F 2002/065: {Y-shaped blood vessels}
- A61F 2002/075: {the stent being loosely attached to the graft material, e.g. by stitching}
- A61F 2220/0075: sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
- A61F 2230/0034: D-shaped
- A61F 2250/0003: having an inflatable pocket filled with fluid, e.g. liquid or gas
- A61F 2250/0039: differing in diameter
- A61F 2250/0071: breakable or frangible
- A61F: FILTERS 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 (dental prosthetics A61C)

## Abstract

An endovascular graft, which is configured to conform to the morphology of a vessel to be treated, includes a tubular ePTFE structure; an inflatable ePTFE structure disposed over at least a portion of the ePTFE tubular structure; and an injection port in fluid communication with the inflatable ePTFE structure for inflation of the inflatable ePTFE structure with an inflation medium. The inflatable ePTFE structure may be longitudinally disposed over the tubular ePTFE structure. The ePTFE structure may be a bifurcated structure having first and second bifurcated tubular structures, where the inflatable ePTFE structure is disposed over at least a portion of the first and second bifurcated tubular structures.

## Claims

### Claim 1

An implantable device, comprising:
a frame structure of biocompatible graft material having first and second opposed open ends, said first opposed open end having a longitudinal axis and a neck portion disposed directly at a terminal portion of said first opposed open end;
a non-inflatable expansion member generally coextensive with the longitudinal axis of said first opposed open end and securably disposed at the neck portion of said frame structure;
an inflatable structure disposed over at least a first portion of said frame structure near said first opposed open end, wherein the inflatable structure is longitudinally spaced apart from the non-inflatable expansion member; and
a fluid for inflating the inflatable structure;
wherein the inflatable structure is inflatable with the inflation fluid to provide an inflated state such that the inflated state conforms to the shape of a bodily lumen.

### Claim 2 (depends on 1)

The device of claim 1, wherein the inflated state conforms to a morphology of a deployment site of a bodily lumen.

### Claim 3 (depends on 1)

The device of claim 1, wherein the biocompatible graft material of the frame structure comprises a polymeric material selected from the group consisting of polyvinylchloride (PVC), polyurethane, polyethylene, polyethylene terephthalate (PET) and fluoropolymer.

### Claim 4 (depends on 3)

The device of claim 3, wherein the fluoropolymer is selected from the group consisting of polytetrafluoroethylene (PTFE) and expanded polytetrafluoroethylene (ePTFE).

### Claim 5 (depends on 1)

The device of claim 1, wherein the inflatable structure comprises a polymeric material selected from the group consisting of polyvinylchloride (PVC), polyurethane and polyethylene.

### Claim 6 (depends on 1)

The device of claim 1, wherein the inflatable structure comprises a polyurethane material.

### Claim 7 (depends on 1)

The device of claim 1, wherein the non-inflatable expansion member is configured to self-expand from a constrained state.

### Claim 8 (depends on 1)

The device of claim 1, wherein the non-inflatable expansion member is configured expand to upon application of an outward radial force.

### Claim 9 (depends on 8)

The device of claim 8, wherein the application of the outward radial force is provided by an inflation member of a balloon catheter.

### Claim 10 (depends on 1)

A system for percutaneous delivery of an implantable device, comprising:
the implantable device of claim 1; and
a delivery catheter.

### Claim 11 (depends on 1)

The device of claim 1, wherein the non-inflatable expansion member comprises an expandable ring having a serpentine configuration.

### Claim 12 (depends on 11)

The device of claim 11, wherein a portion of the serpentine configuration of the non-inflatable expansion member is disposed beyond said first opposed open end of the frame structure.

### Claim 13

An implantable device, comprising:
a frame structure comprising biocompatible graft material having first and second opposed open ends and a metallic reinforcement member, said first opposed open end having a longitudinal axis and a neck portion disposed directly at a terminal portion of said first opposed open end;
an inflatable structure disposed over at least a first portion of said frame structure near said first opposed open end; and
a fluid for inflating the inflatable structure;
wherein the metallic reinforcement member is securably disposed at the neck portion of said frame structure, the metallic reinforcement member being longitudinally spaced apart from the inflatable structure; and
wherein the inflatable structure is inflatable with the inflation fluid to provide an inflated state such that the inflated state conforms to the shape of a bodily lumen.

### Claim 14 (depends on 13)

The device of claim 13, wherein the inflated state conforms to a morphology of a deployment site of a bodily lumen.

### Claim 15 (depends on 13)

The device of claim 13 wherein the biocompatible graft material of the frame structure comprises a polymeric material selected from the group consisting of polyvinylchloride (PVC), polyurethane, polyethylene, polyethylene terephthalate (PET) and fluoropolymer.

### Claim 16 (depends on 15)

The device of claim 15, wherein the fluoropolymer is selected from the group consisting of polytetrafluoroethylene (PTFE) and expanded polytetrafluoroethylene (ePTFE).

### Claim 17 (depends on 13)

The device of claim 13, wherein the inflatable structure comprises a polymeric material selected from the group consisting of polyvinylchloride (PVC), polyurethane and polyethylene.

### Claim 18 (depends on 13)

The device of claim 13, wherein the inflatable structure comprises a polyurethane material.

### Claim 19 (depends on 13)

A system for percutaneous delivery of an implantable device, comprising:
the implantable device of claim 13; and
a delivery catheter.
