Abstract: A closure device for closing a bodily passageway is provided. The device includes first and second frames and first and second crossbars. A sheet of biocompatible material is attached to one or more of the frames. The first crossbar extends across the first frame and has terminal crossbar ends connectively linked to separate sites on the first frame; the second crossbar is similarly linked to the second frame. The crossbars are attached to each other at a connection point, and they are each configured to bend away from the connection point when the closure device is deployed to close a bodily passageway. A method of making the closure device is provided, as well as a method for closing a bodily passageway using such a device. Further, a closure device assembly is provided, including a closure device, a delivery catheter housing, and a delivery release member.

Abstract: A coated implantable medical device 10 includes a structure 12 adapted for introduction into the vascular system, esophagus, trachea, colon, biliary tract, or urinary tract; at least one coating layer 16 posited on one surface of the structure; and at least one layer 18 of a bioactive material posited on at least a portion of the coating layer 16, where the coating layer 16 provides for the controlled release of the bioactive material from the coating layer. In addition, at least one porous layer 20 may be posited over the bioactive material layer 18, where the porous layer includes a polymer and provides for the controlled release of the bioactive material therethrough. Preferably, the structure 12 is a coronary stent. The porous layer 20 includes a polymer applied preferably by vapor or plasma deposition and provides for a controlled release of the bioactive material.

Abstract: A side branch stent graft (1) suitable for the iliac arteries has a main tubular body (3) of a biocompatible graft material and a tubular side branch (5). The tubular side branch is affixed into the main tubular body so that a side branch lumen is in fluid communication with a main lumen. There is at least one external zig-zag stent (13) on the main tubular body proximal of the tubular side branch, one central external stent (14) which also encompasses the side arm, at least one external zig-zag stent (16) on the main tubular body distal of the tubular side branch and one internal zig-zag stent (15) at the distal end of the main tubular body. A reinforcing ring (9) is around the proximal end of the main tubular body and stitched thereto.

Abstract: Prosthetic medical devices with delayed valve function and in situ remodeling of a portion thereof are provided, as well as methods of manufacturing the medical devices and methods of treatment using the medical devices. The medical devices may be adapted to initially maintain a remodelable material within a body vessel in a first configuration suitable to contact the remodelable material with a body fluid contacting the remodelable material for a first time period or a second configuration adapted to regulate the flow of body fluid contacting the remodelable material. The medical devices may include a releasable holding member configured to retain the remodelable material in the first configuration.

Abstract: A guidable cutting instrument for cutting a tissue specimen from a tissue mass comprises a cannula having a curve formed along a distal portion thereof, and a stylet having a specimen-receiving notch and a curve formed along a distal portion thereof. The stylet is received in the cannula, and is axially extendable therefrom such that the notch is capable of penetrating the tissue mass. The cannula is axially movable over the extended stylet for severing the specimen from the mass for capture in the notch. The cannula and stylet are each structured and arranged for relative rotation between a first position wherein the cannula curve and the stylet curve are in phase to define a curved condition for a length of the cutting instrument, and a second position wherein the cannula curve or stylet curve is rotated relative to the other curve in a manner to define a generally linear condition of the cutting instrument.

Abstract: Apparatus for cooling the brain comprises a pernasal intubation tube for insertion through one of the nostrils of a patient requiring brain cooling; an inflatable occluder provided the tube for inflation to occlude the nasopharynx of the patient behind the soft palate of the patient thereby to prevent passage of liquid between the nasal cavities and the mouth of the patient; a nostril closure arranged to cooperate with the pernasal intubation tube; an orifice for introduction of a liquid coolant into the nasal cavities; and a liquid vent for insertion in the other nostril of the patient for controlling venting of liquid coolant from the nasal cavities. Also described herein is a method of cooling the brain of a patient in danger of suffering brain damage comprising occluding the air passage leading from the nasal cavities to the mouth cavity of the patient behind the soft palate of the patient and irrigating the nasal cavities of the patient with a coolant liquid.

Abstract: A thrombus retrieval device has one or more thrombus engaging elements that are movable between a retracted configuration in which they are stowed within the device and a deployed configuration in which they project from the device to snare an adjacent thrombus for removal from a blood vessel.

Abstract: Medical systems, devices and methods are provided for coupling a wire guide to a previously introduced wire guide in intracorporeal procedures, and generally include a supplemental wire guide and a tracking element. The tracking element defines a first passageway and a second passageway. The first passageway is sized to receive the previously introduced wire guide and the second passageway is sized to receive the supplemental wire guide. The supplemental wire guide is attached to the tracking element in a coupled configuration and detached from the tracking element in a decoupled configuration for independent translation of the supplemental wire guide.

Abstract: An intraluminal prosthesis is provided for strengthening a main lumen and a branch lumen in direct fluid communication with the main lumen. The prosthesis may comprise a tubular graft and a flexible stent. The tubular graft may include a flexible body having a wall with a fenestration. The flexible stent may include a body with at least one open space to encourage tissue prolapse. The flexible stent may be configured for intraluminal coupling to the fenestration of the tubular graft, so that the entire prosthesis may be assembled and anchored into a main lumen and a branch lumen with a minimally invasive procedure. The open space may encourage tissue prolapse, which may act to anchor the flexible stent to the branch lumen.

Abstract: Described are methods and systems for modifying vascular valves in order to reduce retrograde blood flow through the valves. Preferred methods include connecting vascular valve leaflets with at least one remodelable material, such that the valve leaflets become fused by the ingrowth of the patient's native tissue. Preferred remodelable materials include collagenous extracellular matrix material, such as small intestine submucosa.

Abstract: A balloon catheter is provided that may be used to dilate hardened regions of a stenosis on a vessel wall. The balloon catheter is provided with cutting elements that extend along a surface of a balloon. At least one bioactive is present, either on the cutting element, within the interior of the balloon, within the material of the balloon or on an outside surface of the balloon. The bioactive is delivered to the vessel wall upon dilation of the balloon.

Abstract: A stent graft 30 has a bare end stent 31 which partially overlaps the next stent 32 with the end 36 of the graft material 34 being shaped to follow the distal peaks 35 of the end stent and the proximal peaks 47 of the next stent. The proximal peaks 37 of the end stent have a greater radius of curvature than the distal peaks 35 of the end stent.

Abstract: A system for anchoring an endoluminal prosthesis comprises a barb. The barb comprises a base, a retractable body extending distally from the base towards a distal anchor, and a hinge disposed between the base and the anchor and spaced apart from the base. The anchor pivots about the hinge between a retracted configuration and an extended configuration. Additional devices, systems, and methods are disclosed.

Abstract: This invention relates to medical devices and an angiotensin II type 2 (AT2) receptor antagonist compound, the medical device being adapted to release the AT2 receptor antagonist compound within a body of a patient. This invention also relates to medical devices and methods of treatment of disease, such as aneurysms and aortic dissection. Medical devices may include coated stents, grafts, stent grafts, balloons and catheters.

Abstract: Medical devices for implantation in a body vessel, and methods of using and making the same, are provided. A medical device includes a support frame having struts and a weakened frame portion, and a remodelable material tensionably attached to the support frame. The weakened frame portion has a first configuration in which the support frame has a first outward radial force and a second configuration in which the support frame has a second, lesser outward radial force. The remodellable material restricts expansion of the frame from a radially compressed configuration to a radially expanded configuration when the weakened frame portion is in the first configuration. The remodelable material can form one or more valve leaflets adapted to regulate fluid flow in a body vessel, such as a vein.

Abstract: An introducer assembly (10) includes a guide wire catheter (12), a pusher element (16), an external manipulation unit (28) and an external sheath (30). The distal end (18) of the pusher element (16) is bonded, with adhesive or other bonding agent (32), to the guide wire catheter (12) so as to fix these components together at the distal end (18) of the pusher element (16). This reduces twisting of the pusher element (16) relative to the guide wire catheter (12) and thus twisting of any implantable medical device carried on the introducer assembly (10). This can reduce incorrect deployment of the implantable medical device and reduce instances of an abortive medical procedure. In addition, such bonding increases the torque resistance of the guide wire catheter (12) and pusher element (16) to reduce overall twisting at the distal end of the introducer assembly (10).

Abstract: A catheter for use in an endoluminal delivery assembly includes a device holding region or element on which there is provided a plurality of flexible fingers extending outwardly therefrom. The fingers act to maintain a device to be deployed in the correct position on the catheter and act to resist deformation of the device during deployment.

Abstract: An embolic protection device for capturing emboli during treatment of a lesion in a blood vessel is presented. This embolic protection device generally comprises a plurality of struts having a predetermined shape and being configured to move between an expanded state for engagement with the blood vessel and a collapsed state for filter retrieval and delivery and a filter portion circumferentially attached to the struts having a proximal end and a distal end; the filter portion extending freely from the proximal end to a closed distal end. The filter portion forms at least one annulus chamber in the expanded state with the closed distal end of each chamber being not coincident to the center longitudinal axis of the blood vessel in order capture emboli in the chambers and to reduce any overall restriction of blood flow through the filter portion.

Abstract: A stent graft deployment device (10) has a tubular fixed handle (34, 36) to be gripped and held by a user and an elongate release handle (30) extending through the fixed handle so that the release handle can be moved through the fixed handle. The deployment device assembly has a pusher (38) and a sheath (18) to cover a stent graft (64) on the pusher. The pusher is connected to the fixed handle and the sheath is connected to the release handle so that retraction of the release handle through the fixed handle causes the sheath to be retracted from the stent graft on the pusher. The fixed handle includes a grip component (34) that grips the pusher and a rotator component (36) that grips a release clamp (48) on the pusher. The release clamp has trigger wires for the release of the stent graft attached to it.

Abstract: A dilator element 30 of a stent introducer apparatus 10 comprises a distal part 36 of soft, flexible material and a proximal part 38 of relatively hard and/or stiff material with a proximal end portion 35 which is tapered.