Abbott Cardiovascular Systems, Inc.

Amaitus, Inc.

Abbott Laboratories Corporation

Alexander Nikanorov

Mikael Trollsas

Syed Faiyaz Ahmed Hossainy

Syed F Hossainy

John E Papp

Michael H Ngo

Boris Anukhin

Dudley Shelton Jayasinghe

Zella Solter

Hugh Zhao

Gregory W Fung

Nianjiong Joan Bei

Danielle D LaFlash

Dudley Jayasinghe

Michael Huy Ngo

Mikael O Trollsas

A temporary expandable tissue support device includes a plurality of helical filaments superimposed on top of one another to form a tubular body. A first end of the tubular body is coupled to an inner shaft, and a second end of the tubular body is coupled to an outer shaft slidably disposed over the inner shaft. Actuation of the inner and outer shafts in a first direction compresses the plurality of filaments thereby radially expanding the tubular body into an expanded configuration adapted to engage and support tissue at a treatment site without obstructing a fluid from flowing past the tubular body. Actuation of the shafts in a second direction opposite the first direction tensions the plurality of filaments thereby radially collapsing the tubular body into a collapsed configuration that is adapted to be delivered to or removed from the treatment site.

Temporary and retrievable expandable member

A medical device includes a polymer stent (or scaffold) crimped to a catheter balloon. The stent, after being expanded from a crimped state by the balloon, provides a crush recovery of about 90% of its expanded diameter after being pinched or crushed by an amount equal to about 50% of the expanded diameter. The stent has a pattern including a W-shaped or W-V shaped closed cell and links connecting the closed cells.

Balloon expanded polymer stent

A method of crimping a stent is disclosed. The stent includes a minimum crimped diameter such that in the minimum crimped diameter, a pair of stent rings, between which marker support structures reside, do not make contact with the marker support structures. The crimped profile of the stent of the present invention can be as small as the crimped profile of a same stent but without the maker support structures.

Method of crimping stent on catheter delivery assembly

A method of manufacturing a stent is disclosed. The stent includes a minimum crimped diameter such that in the minimum crimped diameter, a pair of stent rings, between which marker support structures reside, do not make contact with the marker support structures. The crimped profile of the stent of the present invention can be as small as the crimped profile of a same stent but without the marker support structures.

Method of making a stent

A medical device includes a polymer scaffold crimped to a catheter having an expansion balloon. The scaffold, after being deployed by the balloon, provides a crush recovery of about 90% after the diameter of the scaffold has been pinched or crushed by 50%. The scaffold has a pattern including an asymmetric closed cell connecting links connecting the closed cells.

Crush recoverable polymer scaffolds

A guide wire locking mechanism for a catheter system includes a motion-limiting component adapted to contact a portion of a guide wire and limit the direction of motion that the guide wire can slide therethrough. The motion-limiting component allows the guide wire to slide in one direction when placed in the locking mechanism but prevents the guide wire from moving in the opposite direction. The motion-limiting component can be made from a row of movable teeth having contact surfaces or faces which come in contact with a portion of the guide wire. The teeth are bendable to allow the guide wire to move in one direction but will tighten against the guide wire if one attempts to move the guide wire in an opposite direction.

Guide wire locking mechanism for rapid exchange and other catheter systems

Systems, apparatuses, and methods for evaluating medical device performance are provided. A corresponding method may include deploying an implantable medical device into an apparatus for evaluating performance of an implantable medical device. The apparatus may include a support structure and simulated tissue operatively associated with the support structure. The method may further include manipulating the support structure and/or the simulated tissue to simulate physiological forces on the implantable device.

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Palo Alto, CA, United States of America

Alexander Nikanorov