US2018036122A1PendingUtilityA1
Implantable Valve Prosthesis
Assignee: MEDTRONIC 3F THERAPEUTICS INCPriority: Apr 23, 2004Filed: Aug 24, 2017Published: Feb 8, 2018
Est. expiryApr 23, 2024(expired)· nominal 20-yr term from priority
A61F 2/2418A61F 2230/0013A61F 2220/0075A61L 27/507A61L 27/3882A61F 2/0077A61L 27/18A61L 27/3804A61F 2250/0098A61F 2220/0041A61F 2210/0014A61F 2230/0069A61L 27/26A61F 2250/0069A61L 27/50A61F 2/2409A61L 27/047A61F 2220/005A61L 2430/20A61F 2230/0054A61F 2002/0086A61F 2/04
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Claims
Abstract
The present invention provides valve prostheses adapted to be initially crimped in a narrow configuration suitable for catheterization through body ducts to a target location and adapted to be deployed by exerting substantially radial forces from within by means of a deployment device to a deployed state in the target location.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A prosthetic valve assembly comprising:
an expandable annular stent frame; a valve attached to the expandable annular stent frame; and a seal attached to an outer surface of the expandable annular stent frame, wherein the seal comprises a first cylindrical portion and a second cylindrical portion, the first cylindrical portion having greater thickness than the second cylindrical portion, wherein the first cylindrical portion is disposed adjacent the second cylindrical portion, and wherein a radial lip is defined by an interface of the first cylindrical portion and the second cylindrical portion.
3 . The prosthetic valve assembly of claim 2 wherein the seal comprises a material configured to facilitate tissue ingrowth.
4 . The prosthetic valve assembly of claim 2 wherein the seal comprises a cloth material.
5 . The prosthetic valve assembly of claim 2 wherein the expandable annular stent frame comprises a material selected from the group consisting of memory shaped metals, memory shaped polymers, biocompatible stainless steel and polymeric material.
6 . The prosthetic valve assembly of claim 2 wherein the expandable annular stent frame comprises polyethylene terphthalene.
7 . The prosthetic valve assembly of claim 2 wherein the valve comprises at least two leaflets.
8 . The prosthetic valve assembly of claim 7 wherein the leaflets comprise a material selected from the group consisting of natural tissue and biocompatible materials.
9 . The prosthetic valve assembly of claim 8 wherein the natural tissue is pericardial tissue.
10 . The prosthetic valve assembly of claim 8 wherein the biocompatible material is polyurethane.
11 . The prosthetic valve assembly of claim 2 wherein the expandable annular stent frame is configured to be radially collapsible to a diameter of 4-25 mm.
12 . The prosthetic valve assembly of claim 2 wherein the expandable annular stent frame is configured to be radially expandable to a diameter of 10-33 mm.
13 . The prosthetic valve assembly of claim 2 wherein the valve has a generally tubular shape.
14 . The prosthetic valve assembly of claim 13 wherein the valve has an outer diameter that is 1-5 mm smaller than an inner diameter of the expandable annular stent frame.
15 . The prosthetic valve assembly of claim 2 wherein the valve comprises a tricuspid configuration.
16 . The prosthetic valve assembly of claim 2 wherein the expandable annular stent frame has at least one marker configured to track and determine position and orientation of the prosthetic valve assembly.
17 . The prosthetic valve assembly of claim 16 wherein the at least one marker comprises a metal selected from the group consisting of gold, platinum, iridium, tantalum, cobalt, chrome and titanium alloys.
18 . The prosthetic valve assembly of claim 2 wherein the valve has a radio-opaque material configured to facilitate in vivo tracking of the prosthetic valve assembly.
19 . The prosthetic valve assembly of claim 18 wherein the radio-opaque material comprises gold thread.
20 . The prosthetic valve assembly of claim 2 wherein the seal comprises a cuff.
21 . A prosthetic valve assembly comprising:
an expandable annular stent frame; a valve assembly attached to the expandable annular stent frame; and a seal member attached to an outer surface of the expandable annular stent frame, wherein the seal member comprises a first cylindrical portion and a second cylindrical portion, the first cylindrical portion having greater thickness than the second cylindrical portion, wherein the first cylindrical portion is disposed downstream of the second cylindrical portion, and wherein a radial lip is defined by an interface of the first cylindrical portion and the second cylindrical portion.Join the waitlist — get patent alerts
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