Braided scaffolds

US10004834B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10004834-B2
Application numberUS-201414484943-A
CountryUS
Kind codeB2
Filing dateSep 12, 2014
Priority dateSep 13, 2013
Publication dateJun 26, 2018
Grant dateJun 26, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A braided polymeric scaffold, made at least in part from a bioresorbable material is deployed on a catheter that uses a push-pull mechanism to deploy the scaffold. A drug coating is disposed on the scaffold. A plurality of scaffold segments on a catheter is also disclosed.

First claim

Opening claim text (preview).

What is claimed is: 1. A self-expanding stent for treating a peripheral vessel, comprising: a segmented braided scaffold including a plurality of braided scaffold segments configured to be deployed end to end in a vessel, and at least three of the braided scaffold segments are hybrid segments, each of which comprising non-degradable filaments and degradable filaments woven to form a tubular configuration, wherein upon deployment of the scaffold from a collapsed state to a deployed state in a body cavity, the degradable filaments degrade and a radial strength or stiffness of the hybrid segments decreases with time, wherein when the degradable filaments are completely degraded, each hybrid segment comprises a residual stiffness provided by the non-degradable filaments, and wherein a hybrid proximal end segment a hybrid distal end segment of the scaffold have a higher radial strength or stiffness at deployment than a middle hybrid segment thereof, while having the same residual radial strength or stiffness as the middle hybrid segment, and wherein a first degradable polymer filament of the proximal and distal hybrid end segments has a higher degradation rate than a second degradable polymer filament of the middle hybrid segment so that a rate of decrease to the residual strength or stiffness is faster for the proximal and distal hybrid end segments than the middle hybrid segment. 2. The stent of claim 1 , wherein the non-degradable filaments are nitinol. 3. The stent of claim 1 , wherein the degradable filaments comprise a polymer selected from the group consisting of poly(L-lactide), poly(L-lactide-co-glycolide), poly(DL-lactide), and polyglycolide. 4. The stent of claim 1 , wherein the degradable filaments comprise a bioabsorbable polymer. 5. The stent of claim 1 , wherein the radial strength or stiffness of at least one of the hybrid end segments decreases by no greater than 60% during the first 3 months after deployment. 6. The stent of claim 1 , wherein the radial strength or stiffness of at least one of the proximal and distal hybrid end segments decreases by at least about 50% during the first 3 months after deployment. 7. The stent of claim 1 , wherein the stiffness of at least one of the proximal and distal hybrid end segments decreases to 40 to 60% of a stiffness at deployment during the first 3 months after deployment. 8. The stent of claim 1 , wherein the stiffness of at least one of the proximal and distal hybrid end segments decreases to a residual stiffness that is less by 40% to 60% of a deployed stiffness, by at least 3 months after deployment. 9. The stent of claim 1 , wherein a combined length of the distal and proximal hybrid end segments are 10% to 30% of a total length of the scaffold. 10. The stent of claim 1 , wherein one of the hybrid proximal end segment and hybrid distal end segment comprises a metal filament having a cross sectional area (Am), and a degradable filament having a cross-sectional area (Ap), wherein the ratio Ap/Am is 2 to 4. 11. The stent of claim 1 , wherein one of the hybrid proximal end segment and hybrid distal end segment comprises a number of metal filaments (Nm) and a number of polymer filaments (Np), wherein the ratio Np/Nm is 2 to 10.

Assignees

Inventors

Classifications

  • differing in diameter · CPC title

  • A61L31/148Primary

    Materials at least partially resorbable by the body · CPC title

  • differing in elasticity, stiffness or compressibility · CPC title

  • characterised by a net-like or mesh-like structure · CPC title

  • containing other specific inorganic fillers not covered by A61L31/126 or A61L31/127 · CPC title

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Frequently asked questions

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What does patent US10004834B2 cover?
A braided polymeric scaffold, made at least in part from a bioresorbable material is deployed on a catheter that uses a push-pull mechanism to deploy the scaffold. A drug coating is disposed on the scaffold. A plurality of scaffold segments on a catheter is also disclosed.
Who is the assignee on this patent?
Abbott Cardiovascular Systems Inc
What technology area does this patent fall under?
Primary CPC classification A61L31/148. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).