Cook Incorporated

Suros Surgical Systems, Inc.

Cook Medical Technologies LLC

Other

Hologic, Inc.

Med Institute Incorporated

Cook Critical Care Incorporated

Cook Incorporated and Sabin Corporation

William Cook Europe Aps

Michael C Hoffa

Scott E Boatman

Darin Gene Schaeffer

David G Burton

Joseph L Mark

Michael E Miller

Brian L Bates

David A Drewes

David R Lessard

Maggie A Z Hupcey

Thomas A Osborne

Anthony O Ragheb

Zachary R Nicoson

Jason S Sturgeon

Jacob A Flagle

Terry D Hardin

William O Hodge

Justin Smith

Kimberly D Roberts

Inderjeet S Jarial

Jason M Butcher

Neal E Fearnot

William D Voorhees, Iii

Daniel J Sirota

Arthur B Fontaine

Jason C Urbanski

Coy M Herald

Bruce Gingles

Dale T Berry

Susan DosPassos

Michael Miller

Inderjeet Jarial

Terry Hardin

A coated medical device () including a structure () adapted for introduction into a passage or vessel of a patient. The structure is formed of preferably a non-porous base material () having a bioactive material layer () disposed thereon. The medical device is preferably an implantable stent or balloon () of which the bioactive material layer is deposited thereon. The stent can be positioned around the balloon and another layer of the bioactive material posited over the entire structure and extending beyond the ends of the positioned stent. The ends of the balloon extend beyond the ends of the stent and include the bioactive material thereon for delivering the bioactive material to the cells of a vessel wall coming in contact therewith. The balloon further includes a layer of hydrophilic material () positioned between the base and bioactive material layers of the balloon.

Coated medical device

A stent deployment device () is provided for deploying a stent in a lumen of a patient. The device can include a catheter (), a first balloon () positioned near a distal end of the catheter and a second balloon () adjacent to the first balloon. Alternatively, the second balloon can be positioned over the first balloon. The device also includes an expandable stent () positioned over the first balloon and the second balloon. The first balloon comprises a semi-compliant material, a noncompliant material or a compliant material. Similarly, the second balloon comprises a semi-compliant material, a noncompliant material or a compliant material. The first balloon is expandable to a first diameter, while the second balloon can be expandable to a second diameter.

Stent deployment device

A stent graft system for intraluminal deployment in an aorta and a branch vessel that includes an aorta stent graft for deployment within the aorta and defining a lumen for the passage of blood therethrough, and having a fenestration positioned and sized so as to allow blood to flow to a contiguous branch vessel. The system also includes a branch vessel prosthesis, preferably a stent graft, having a tubular portion and a flaring portion, such that, when deployed, the flaring portion is located within the lumen of the aorta stent graft and the tubular portion passes through the fenestration and into the branch vessel. A balloon expansion catheter expands the tubular portion and flare the flaring portion. The expansion of the tubular portion and the flaring of the flaring portion may occur sequentially or simultaneously.

Balloon flareable branch vessel prosthesis and method

A surgical device is disclosed that comprises a cutting element, a biopsy line, a motor line, and a vacuum line. The cutting element includes an outer cannula and an inner cannula. The biopsy line is operatively connected to a control console for moving the inner cannula within the outer cannula to cut tissue cores. The motor line is operatively connected to the control console for operating the surgical device. The vacuum line is operatively connected to the inner cannula. A selectively openable tissue filter is operatively connected to the inner cannula, and is also connected to the vacuum line.

Surgical system

A biopsy device having a cutting element is disclosed. The cutting element includes an inner cannula having a tissue receiving aperture disposed proximate a distal end thereof and an inner lumen. The inner cannula is slidably disposed within the inner lumen of an outer cannula. A vacuum chamber is disposed about at least a portion of the cutting element and is configured to create a vacuum in the cutting element during a biopsy procedure. The inner cannula is advanced distally outwardly and to cause the vacuum to be generated in the vacuum chamber. The vacuum is delivered to the cutting element whereby tissue is drawn into the tissue receiving aperture. The outer cannula is advanced distally outwardly after the inner cannula such that tissue drawn into the tissue cutting aperture is severed.

Vacuum assisted biopsy needle set

A target localizing and marking device is provided including a cannula having proximal and distal ends and a lumen therebetween, and a tip member releasably attached to the distal end, where the tip member includes and outer shell and at least one inner chamber. The device further includes at least one image enhancing component disposed on the outer shell and/or within the at least one inner chamber, at least one marking component disposed in the at least one inner chamber, and a tip member deployment mechanism. The deployment mechanism has a manually engageable actuator, a portion of which is dimensioned to slidably pass through the lumen of the cannula, and is operable to separate the tip member from the cannula and deploy the tip member to a predetermined target site. In some implementations, the device is magnetic resonance imaging (MRI) compatible and is identifiable under MRI.

Localizing obturator with site marking capability

A branch vessel prosthesis for use with an aorta stent graft defining a lumen and having a fenestration aligned with a branch vessel, includes an expandable stent that has a tubular portion, a flareable portion, and at least one bending portion located between the tubular and the flareable portions. Upon deployment of the branch vessel prosthesis, the flareable portion is flared by bending of the bending portion.

Flareable branch vessel prosthesis and method

A site marker is provided that includes a generally hollow body defining a cavity. At least one marker element is captured within the cavity but is able to move within the cavity. The capturing prevents migration of the marker within a body. The site marker is formed into a predeployment configuration whereby the site marker is compressed into a predetermined size and shape to as to be readily positionable within a deployment device. The site marker expands from the predeployment position to a post deployment configuration upon insertion into the body.

Site marker visable under multiple modalities

A coated medical device adapted for introduction into a passage or vessel of a patient is provided. The medical device is preferably an implantable balloon with a bioactive deposited or within the balloon. The balloon can further include a hydrophilic material positioned between the balloon and a bioactive material posited on the balloon.

A medical device () including a catheter shaft () and a unitarily and continuously formed portion () having a varying durometer, and optionally including an expandable balloon (). One or both of the unitarily and continuously formed portion () and the balloon () are made from an irradiation cross-linked or cross-linkable mixture of a polyamide elastomer and at least one additional cross-linking reactant. The polyamide elastomer can be a polyester amide, a polyether ester amide or a polyether amide, and is preferably a nylon block copolymer. The aromatic molecule can be 1,3,5 triethyl benzene; 1,2,4 triethyl benzene; and 1,3,5 triisopropyl benzene. The cross-linking reactant can be: (a) a difunctional material, (b) a trifunctional material, (c) a tetrafunctional material, or (d) an aromatic molecule containing at least two ring substituents, each of the ring substituents having labile hydrogens at a benzylic site therein. The cross-linking reactant can also be diallyl phthalate or meta-phenylene dimaleimide.

Medical device including unitary, continuous portion of varying durometer

An apparatus and method for inserting an article into a body opening. A radially expandable introducer sheath is delivered in a non-expanded condition into a body opening. A release mechanism releases the introducer sheath from the non-expanded condition into a condition that permits radial expansion of the introducer sheath upon introduction of a medical device through the sheath into the body opening. An optional handle having a circumferential opening may be provided for withdrawing the sheath from the body opening, while leaving the medical device in place.

Introducer sheath

A medical device () includes a catheter shaft () including inner and outer catheter shafts (and), and an expandable balloon () carried by the catheter shaft (). The balloon () is made from an irradiation cross-linked mixture of a polyamide elastomer and at least one additional cross-linking reactant. The polyamide elastomer can be a polyester amide, a polyether ester amide or a polyether amide, and is preferably a nylon block copolymer. The cross-linking reactant can be: (a) a difunctional material, (b) a trifunctional material, (c) a tetrafunctional material, or (d) an aromatic molecule containing at least two ring substituents, each of the ring substituents having labile hydrogens at a benzylic site therein. The cross-linking reactant can also be diallyl phthalate or meta-phenylene dimaleimide. Irradiation is carried out by exposure to an electron beam or to ultraviolet, X- or gamma radiation, preferably at a total fluence of about 0.5 to about 20 megarads. The amount of the cross-linking reactant is selected to avoid the formation of gelling during the process by which the balloon () is made, and the amount of the cross-linking agent and the irradiation fluence are selected to give the balloon a strength generally about equal to that which would be obtained by mere irradiation.

Medical device including improved expandable balloon

Growing community of inventors

Brownsburg, IN, United States of America

Michael C Hoffa