Medtronic, Inc.

Biomedical Device Consultants and Laboratories of Colorado, LLC

Advanced Cardiovascular Systems, Inc.

Medtronic Ave, Inc.

Medtronics, Inc.

Biomedical Device Consultants & Laboratories LLC

Vascular Devices LLC

Steven Weinberg

Jay Alan Lenker

Michael A Evans

Brian J Cox

Craig Weinberg

Benjamin McCloskey

Thomas J Fogarty

Steven W Kim

Kirsten Freislinger

Anthony J Bradshaw

Albert E Raizner

A fatigue testing system provides simultaneous cycle testing for a plurality of prosthetic devices under simulated physiological loading conditions. A plurality of sample holders containing test samples of prosthetic devices is positioned between a distribution chamber and a return fluid chamber to form an integrated test chamber. A reciprocating linear drive motor operates a rolling bellows diaphragm to cyclically pressurize fluid within the test chamber and drive the pressurized fluid through the prosthetic devices being tested. The test chamber defines a return flow conduit in fluid communication with each of the sample holders, the return fluid chamber, and the distribution chamber. Compliance chambers and throttle valves associated with each of the sample holders regulate the pressure gradient and back pressure across the prosthetic devices being tested.

Fatigue testing system for prosthetic devices

Prostheses are fatigue tested using an apparatus under simulated physiological loading conditions. A fluid housing defines an entrance chamber having fluid outflow ports and an exit chamber having opposing fluid inflow ports and a central flow conduit in communication with the entrance chamber and the exit chamber. A plurality of housing tubes into which prosthesis are deployed may extend between the fluid outflow and inflow ports. Alternatively, tubular prostheses may be connected directly between the inflow and outflow ports. A reciprocating linear drive pump having a flexible diaphragm is provided to cyclically pressurize fluid through a common closed loop within the fluid housing and drive the pressurized fluid through the prosthesis being tested. The test system is capable of rotation independent of the motor drive for accurate diameter measurements of all test samples at elevated frequencies.

Fatigue evaluation of prostheses by radial excitation of tubular structures

The present invention relates to a segmental self-sealing graft for implantation in a patient including a base tubing element, a tubular access element overlying the base tubing, and a strand-like compression element wound over the access element so as to provide radially inward compression, and a method of making same.

Self-sealing vascular graft

The present invention provides controlled expansion endoluminal prostheses and methods for their deployment and expansion. The present stent-grafts generally comprise a radially expansible tubular frame and a plastically expansible liner on the frame. Either the frame or the liner includes a reinforcing element which limits expansion of the stent-graft at a predetermined expanded size. In some embodiments, the reinforcing element restrains the frame, for example, by limiting the circumferential diagonals of perforations on a perforate frame structure. Generally, however, the reinforcing element is included in the liner as circumferentially oriented yarn. A particularly advantageous liner includes composite circumferential yarns having inexpansible fibers wrapped around an expansible fiber, such as a partially oriented yarn, PTFE, or the like.

Cuffed endoluminal prosthesis

A source wire having a radioactive source at its distal tip is used to treat a blood vessel within a patient's body by localized in vivo radiation to prevent stenosis of the blood vessel, including restenosis following percutaneous transluminal coronary angioplasty. The source wire is advanced to the target site along the intravascular system of the patient's body from a point external to the body. The source wire is preferably a solid lead of substantially uniform thickness along its entire length, composed of a superelastic nickel-titanium alloy (nitinol). Alternatively, the wire may be a cable composed of multiple strands of the alloy of substantially uniform thickness throughout the entire length of each strand. The alloy has desired characteristics of superelasticity for transitioning into and out of a stress-induced martensitic state as it is advanced through tortuous lumens for passage into the coronary arteries. The wire also is of a diameter suitable for passage into the coronary arteries, and the distal end of the wire may be tapered for ease of entry into narrowed portions. The targeted tissue is irradiated only briefly, with the radioactive source of the source wire positioned in the lumen of the coronary artery so as to deliver a substantially uniform dosage of radiation to the walls of the lumen.

Radioactive source wire, apparatus and treatment methods

The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or &ldquo;prosthetic modules,&rdquo; may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.

Modular intraluminal prosteheses construction and methods

Limited expansion endoluminal prostheses and methods for their use

The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or 'prosthetic modules,' may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.

Stitched stent grafts and methods for their fabrication

Method for deploying cuff prostheses

Modular intraluminal prostheses construction and methods

Growing community of inventors

League City, TX, United States of America

Steven Weinberg