Medtronic Vascular, Inc.

Medtronic, Inc.

James Mitchell

Justin Peterson

Victoria Ung

Dustin Thompson

Syamala Rani Pulugurtha

Jill Mendelson

Ryan Bienvenu

Joseph Traina

Nathanael Glucklich

Christopher W Storment

Jeffrey W Allen

Dishuan Chu

William W Chang

Martha Barajas-Torres

Siyan Som

Nate Glucklich

Rajen Kumar

Abby Schlichting

Matthew Rust

Don H Tran

Trevor Greenan

William Berthiaume

Joseph Berglund

Ya Guo

Brian Castelli

Leonel Mendoza

David Grossman

Salvador Avelar

Frank Yang

Ashley Spink

Abby S Pandya

Robert H Murray

Justin Goshgarian

Kshitija P Garde

Gianfranco Pellegrini

Michele Lee Silver

Stuart Earl Kari

Leonila Rivera

Heath Muzslay

Terry Morgan

Mark Casley

Syed Askari

Karl L Olney

Brian Cook

Shahnaz Javani

Philip C Leung

Genevieve E Farrar

Ethan Korngold

Natividad Vasquez

Joe Traina

William Heaton

Eric Yu

Leo Mendoza

Veronica Woen

Priyanka Ganesh

Nirav P Patel

Andrew Czyzowski

Biodegradable magnesium alloy implantable medical devices are protected to delay onset of corrosion, and thus biodegradability, or to corrode more uniformly. The protection allows for extended effective use of the devices while maintaining biodegradability. Examples of protective coatings include conversion coatings that at least partially remove exposed second phases from a surface of the magnesium alloy and coatings that provide a barrier between water and the surface of the magnesium alloy.

Protected magnesium alloys for bioresorbable stents

A system for assisting in loading an implantable medical device onto a delivery system includes a body having a first end, a second end, and a conduit extending from the first end to the second end. The body has an inner diameter that allows a distal portion of the delivery system to slidably move through the conduit. The body has an outer diameter that allows the body to be inserted into a central lumen of the implantable medical device.

Methods and systems for delivery device insertion during medical device crimp processes

A catheter includes a handle with torqueing and steering mechanisms. The torqueing mechanism includes a rotatable nosecone and a bearing coupled to the nosecone to be rotatable therewith. The bearing is concentrically disposed over a shaft of the catheter. The steering mechanism includes a rack coupled to the bearing to be slideable therewith and a pull wire having a proximal end attached to the bearing and a distal end attached to a distal portion of the shaft. Rotation of the nosecone causes an entire length of the shaft to rotate and axial movement of the rack tensions the pull wire to bend the distal portion of the shaft. A valve relief component is slidingly disposed over the shaft and is configured to dock onto the handle when not in use.

Catheter handle with torque mechanism and valve relief component

A crimper for altering an implantable medical device from an uncompressed state to a compressed state. The crimper includes a plurality of crimper elements that define a crimper channel, each of the crimper elements including a non-planar surface that forms a portion of the crimper channel. Each non-planar surface is configured to apply non-uniform radial compression along a length of the implantable medical device during operation of the crimper when altering the implantable medical device from the uncompressed state to the compressed state. The crimper also includes handle configured to operate the crimper. Actuation of the handle decreases a volume of the crimper chamber to transition the implantable medical device from the uncompressed state to the compressed state.

Iris-style crimpers for medical devices

A transcatheter valve prosthesis includes a stent having a crimped configuration for delivery within a vasculature and an expanded configuration for deployment within a native heart valve. The stent includes at least one axial frame member. The transcatheter valve prosthesis includes at least one outflow marker positioned on the at least one axial frame member. The transcatheter heart valve prosthesis may include inflow markers positioned within the inflow portion of the stent. The transcatheter heart valve prosthesis may include two outflow markers disposed on axial frame members and being circumferentially and longitudinally offset from each other. The markers are configured to aid in axial and circumferential aligned of the transcatheter heart valve prosthesis within a native heart valve.

Devices and methods for multi-alignment of implantable medical devices

Novel tools and techniques are provided for implementing protection of at least one tissue layer of a medical device or implant during crimping of the medical device or implant. In various embodiments, an implant tissue protection tool may include an outer portion configured to surround one or more outer segments of at least one tissue layer of a medical device to be implanted into a body of a subject and at least one protrusion (which may be affixed to a surface of the outer portion) configured to minimize or prevent occurrence (or likelihood of occurrence) of the at least one tissue layer (in some cases, leaflet material, or the like) of the medical device passing through at least one opening defined by a frame structure of the medical device during crimping of the medical device by a crimping device in preparation for implantation into the body of the subject.

Implant tissue protection tool

Delivery devices for delivery of a stented prosthetic heart valve. Various delivery devices include an outer sheath assembly including an outer sheath connected to a capsule that is advanced proximally to retain the prosthetic valve, which is secured over an inner shaft assembly of the delivery device. The delivery device further includes a bumper to provide a smooth transition of the capsule over the prosthetic valve during loading and recapture procedures. The bumper is expandable from a first position to a second position in which a distal end of the bumper is expanded to increase its diameter. The bumper can be biased in the second, expanded position so that the bumper automatically transitions to the expanded position upon retraction of the outer sheath.

Stented prosthetic heart valve delivery system having an expandable bumper

A catheter based balloon enabled prosthetic heart valve delivery device is provided. The balloon enabled delivery device is configured to deploy a prosthetic heart valve through inflation. The balloon enabled delivery device is further configured to reduce or prevent migration of the prosthetic heart valve during deployment. Migration is prevented through a combination of balanced inflation of the balloon, inflation fluid flow balancing structures, retention rings, retention covers, and balloon surface treatments.

Balloon expandable transcatheter valve deployment devices and methods

A medical device having a first portion, a second portion, and at least one connector connecting the first and second portion is formed using additive manufacturing. The method includes forming a plurality of layers of a first portion of the medical device, placing a first removable masking plate over the first portion with an opening of the masking plate aligned with a point of the first portion, forming at least one layer of a first connector on the first portion, wherein the first connector is formed in the opening of the removable masking plate, forming a plurality of layers of a second portion of the medical device, wherein a first layer of the plurality of layers of the second portion is formed partially on the first connector and partially on the removable masking plate, and removing the first removable masking plate.

Method of making a medical device using additive manufacturing with a masking plate

A method of making a medical device includes forming a precursor medical device using additive manufacturing. The precursor medical device includes a first portion, a second portion, a first connector, and a second connector. The first connector connects the first portion to the second portion and is configured to remain. The second connector connects the first portion to the second portion and are configured to be removed. The second connector is formed such that the second connector is less ductile than the first portion, the second portion, and the first connector. The precursor medical device is processed to remove the second connector without adversely affecting the first portion, the second portion, and the first connector.

Method of making a medical device using additive manufacturing

A stent is formed from a wire having an outer member, a radiopaque member lining at least a portion of the outer member inner surface, and a lumen defined by the outer member inner surface or the radiopaque member inner surface. A substance is disposed in the lumen to be eluted through at least one opening disposed through the outer member to the lumen. The radiopaque member may be substantially continuous along the length of the wire or disposed only along portions of the wire such as crowns. In a method for making the stent, a composite wire including an outer member, a radiopaque intermediate member, and a core member is shaped into a stent pattern and processed to remove the core member and optionally portions of the radiopaque intermediate member, without damaging the outer member.

Hollow drug-filled stent and method of forming hollow drug-filled stent

Methods and apparatus are disclosed for filling a therapeutic substance or drug within a hollow wire that forms a stent. The stent is placed within a chamber housing a fluid drug formulation. During filling, the chamber is maintained at or near the vapor-liquid equilibrium of the solvent of the fluid drug formulation. To fill the stent, a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is filled with the fluid drug formulation via capillary action. After filling is complete, the stent is retracted such that the stent is no longer in contact with the fluid drug formulation. The solvent vapor pressure within the chamber is reduced to evaporate a solvent of the fluid drug formulation. A wicking means may control transfer of the fluid drug formulation into the stent.

Apparatus and methods for filling a drug eluting medical device via capillary action

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Windsor, CA, United States of America

James Mitchell