IP Library Granted Patent US 11,116,650
Granted Patent B2
US 11,116,650 · App. 16/367,906 · Granted Sep 14, 2021

Supra aortic access modular stent assembly and method

Inventors: Keith Perkins (Santa Rosa, CA); Zachary Borglin (Santa Rosa, CA); Mark Stiger (Santa Rosa, CA); Julie Benton (Santa Rosa, CA); Steven Claessens (Santa Rosa, CA); Travis Rowe (Santa Rosa, CA); Mark Young (Santa Rosa, CA)
Assignee: Medtronic Vascular, Inc.
A61F2/852A61F2/07A61F2002/067A61F2250/0063
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Quick Facts
Patent No.
US 11,116,650
App. No.
16/367,906
Granted
Sep 14, 2021
Kind
B2
Abstract

The techniques of this disclosure generally relate to a modular stent device that is deployed via supra aortic access through the brachiocephalic artery. The modular stent device is a base or anchor component to which additional modular stent devices can be attached to exclude diseased areas of the aorta while at the same time allowing perfusion of the left common carotid artery and the left subclavian artery.

Claims (28)

1. An assembly comprising:

a first modular stent device comprising:

a main body;

a bypass gate directly coupled to and extending distally from a distal end of the main body; and

an artery leg directly coupled to and extending distally from the distal end of the main body,

wherein the artery leg has a greater radial force than a radial force of the bypass gate,

wherein the main body has a first longitudinal axis, the bypass gate has a second longitudinal axis, and the artery leg has a third longitudinal axis, the first, second, and third longitudinal axes are parallel with one another when the first modular stent device is in a relaxed configuration;

a second modular stent device configured to be coupled inside the bypass gate, wherein the second modular stent device comprises:

a main body, wherein the main body of the second modular stent device is configured to be deployed within the bypass gate of the first modular stent device;

a bypass gate extending from the main body of the second modular stent device; and

an artery leg extending from the main body of the second modular stent device; and

a tube graft configured to be deployed within the bypass gate of the second modular stent device.

2. The assembly of claim 1 wherein the bypass gate of the second modular stent device is configured to point away from the first modular stent device.

3. The assembly of claim 1 wherein the artery leg of the first modular stent device is configured to be deployed in a brachiocephalic artery.

4. The assembly of claim 1 wherein the artery leg of the second modular stent device is configured to be deployed in a left subclavian artery.

5. The assembly of claim 1 wherein the artery leg of the second modular stent device is configured to be deployed in a left common carotid artery.

6. The assembly of claim 1 further comprising a proximal cuff configured to be coupled to and extend proximally from the main body of the first modular stent device.

7. The assembly of claim 1 wherein the main body of the first modular stent device has a first diameter and the bypass gate of the first modular stent device has a second diameter, the first diameter being greater than the second diameter.

8. The assembly of claim 7 wherein the artery leg of the first modular stent device has a third diameter, the second diameter being greater than the third diameter.

9. The assembly of claim 8 wherein the first diameter is greater than the second diameter and third diameter combined.

10. The assembly of claim 1 wherein the main body of the first modular stent device has a first diameter within a range of 20 mm to 60 mm.

11. The assembly of claim 1 wherein the bypass gate of the first modular stent device has a second diameter within a range of 10 mm to 46 mm.

12. The assembly of claim 1 wherein the artery leg of the first modular stent device has a third diameter within a range of 5 mm to 24 mm.

13. The assembly of claim 1 wherein the artery leg of the first modular stent device is longer than the bypass gate of the first modular stent device.

14. The assembly of claim 1 wherein the artery leg of the first modular stent device has a third length greater than a second length of the bypass gate of the first modular stent device.

15. The assembly of claim 1 wherein the main body of the first modular stent device has a first length within a range of 10 mm to 160 mm.

16. The assembly of claim 1 wherein the bypass gate of the first modular stent device has a second length within a range of 10 mm to 240 mm.

17. The assembly of claim 1 wherein the artery leg of the first modular stent device has a third length within a range of 30 mm to 400 mm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2019
From: PERKINS, KEITH; BORGLIN, ZACHARY; STIGER, MARK; BENTON, JULIE; CLAESSENS, STEVEN; ROWE, TRAVIS; YOUNG, MARK
To: MEDTRONIC VASCULAR, INC.
Reel/Frame 050621/0886 →
Continuity (1)
Related Publication 20200306064A1 · Oct 1, 2020
Cited By (1)
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