Abstract: A lightweight portable device allows a user to accomplish both the exercises of a functional cable machine and a bodyweight suspension trainer. The device can include at least one non-elastic cord or strap, each retractably attached to a reel. The reel has a locking mechanism and a variable resistance mechanism. When the locking mechanism is engaged, it keeps the strap or cord in a fixed location. This allows the user to perform bodyweight suspension training exercises. The variable resistance mechanism of the reel can increase or decrease the amount of force that is needed to be applied to move the reel, thus giving the user the ability to perform the variable resistance exercises of a functional cable machine. The resistance mechanism can be designed as compact and lightweight, thus making the device able to be portable and compact in size.

Abstract: A medical grasping device (10) for vascular use, having an outer sheath (12), an elongate control member (50) extending within an outer sheath (12) to a distal tip section (54), and a proximal control assembly (22) including an actuation section (24) joined to the elongate control member (50). Adjacent to the distal tip section (54) is a grasping portion (70, 70?) that is extendable from the outer sheath (12) to create loops (74, 74?) for grasping a target object (T) for repositioning within the vascular system, or for removal from the patient, with loops being retractable into the outer sheath to hold the target object against the device (10) during movement of the device. Elongate control member (50) is preferably a cannula or tube having a lumen (58) extending completely therethrough for placement over a guide wire (28) already in the patient.

Abstract: An intraoperative anastomosis method is described and comprises the steps of providing an intraluminal prosthesis having a first end and a second end; suturing a first vessel to a second vessel to form a vessel junction; intraluminally delivering the prosthesis so that the first end of the prosthesis is disposed within the first vessel and the second end of the prosthesis is disposed within the second vessel; and deploying the prosthesis so that the prosthesis overlaps and reinforces the vessel junction. The vessel suturing, prosthesis delivering, and prosthesis deploying steps may be performed in a single operation. Other devices, systems, and methods are described.

Abstract: An apparatus and method for endovascular removal of a cardiac valve having at least two valve cusps is disclosed. The apparatus is insertable through a blood vessel to access the cardiac valve. The apparatus includes a first catheter assembly for insertion into a blood vessel, deployable cutting means for cutting at least one valve cusp of the cardiac valve, and a deployable filter assembly disposed adjacent the distal end of the first catheter assembly. The first catheter assembly has a longitudinal axis and a distal end. The cutting means is attached to the distal end of the first catheter assembly. The filter assembly is operable to collect the severed valve cusps and is collapsible for removal from the blood vessel with the severed valve cusps retained therein.

Abstract: A stent graft (40) has a tubular body with a first bifurcation (54) with first and second legs (50, 52) extending from the bifurcation. One of the legs (52) has a further bifurcation (62) to define a side arm. The stent graft can be deployed into the vasculature of a patient with the tubular body being in an aorta of the patient, a first leg extending down an iliac artery, a second leg being directed towards a contralateral iliac artery and the side arm directed to an internal artery of one of the iliac arteries.

Abstract: An apparatus for insertion into a blood vessel and for modulating the baroreflex system of a mammal includes an expandable support member for engaging a wall of a blood vessel at a desired location where baroreceptors are located, and at least one electrode connected with the expandable support member. The at least one electrode is arranged to selectively deliver electric current to modulate the baroreceptors. The apparatus further includes an insulative material attached to at least a portion of the expandable support member for isolating blood flowing through the vessel from the electric current delivered by the at least one electrode.

Abstract: A modular stent graft assembly (10) for repairing a ruptured abdominal aorta aneurysm (90) and having an aortic section tubular graft (12) and an iliac section tubular graft (14). The aortic section graft has a proximal attachment stent (32) thereon for suprarenal attachment of the assembly (10) to the aorta. A proximal end portion (50) of the iliac section graft (14) underlies the distal end portion (28) of the aortic graft (12) and presses outwardly thereagainst forming a friction fit, at a telescoping region (64). The assembly (10) can be selected from an inventory (300) containing a set of delivery systems (100) of four size aortic section grafts (12) and a set of delivery systems (200) of four size iliac section grafts (14), that together accommodate a large majority of aneurysm sizes, and delivery systems (250) containing four standard sizes of occluders (80).

Abstract: A stent graft introducer has a pusher, a nose cone, a region between the pusher and the nose cone for a stent graft, a sleeve extending over the pusher and proximally to the nose cone to cover the stent graft when retained in the region. An indwelling auxiliary catheter with a pre-curved proximal end is fitted into the introducer. The nose cone has an elongate groove and the auxiliary catheter has its proximal end in the elongate groove. In a partially retracted position of the sleeve the curved proximal end of the indwelling auxiliary catheter is exposed and uncovered by the sleeve and in an advanced position of the sleeve the curved proximal end of the indwelling auxiliary catheter is straightened, extends along the length of the groove in the nose cone and is covered by the sleeve.

Abstract: A stent graft delivery system in which a stent graft (6) is retained on a delivery device (2) such that a longitudinal portion of the stent graft is releasably retained on the delivery device to bend therewith. The delivery device (2) has a guide wire catheter (3) and the stent graft is retained onto the guide wire catheter by a release wire (24) which can be withdrawn. The release wire is wound around the guide wire catheter and through the stent graft or suture loops engage around the guide wire catheter and release wire.

Abstract: A medical device that may be implanted intraluminally in a patient includes a stent and a filter combination. In one variation, the device includes a stent with a distal portion adapted to capture particles during the placement of the device in a stenosed region within a blood vessel. In another variation, the device includes a collapsible filter positioned within the distal lumen of the stent.

Abstract: An aortic stent graft and a method of deploying the aortic stent graft. The method comprises providing a tapered tubular graft having a distal end and a proximal end, providing at least one stent attached to the graft at a site adjacent the distal end of the graft, loading the graft into an introducer, inserting the introducer through an incision in the aorta, deploying the graft inside the aorta; and suturing the proximal end of the graft in place.

Abstract: An apparatus for repairing the function of a diseased valve includes an annular first support member expandable to a first diameter. An annular second support member is spaced axially apart from the first support member and is expandable to a second diameter that is independent of the first diameter. A tubular graft section interconnects the first and second support members. The graft section defines an annulus having a third diameter that is independent of each of the first and second diameters. A prosthetic valve is secured within the annulus of the graft section. The bioprosthetic valve has at least two valve leaflets that are coaptable to permit the unidirectional flow of blood. Methods for repairing the function of a diseased valve and for making the apparatus are also provided.

Abstract: An endoluminal prosthesis comprises a prosthetic trunk comprising a trunk lumen extending therethrough, a wall, an anastomosis in the wall, and a first fenestration in the wall, wherein the prosthetic trunk has a circumference. The endoluminal prosthesis further comprises a prosthetic branch comprising a branch lumen extending therethrough. The branch lumen is in fluid communication with the trunk lumen through the anastomosis. The prosthetic branch is disposed longitudinally along and circumferentially about the prosthetic trunk.

Abstract: A data storage and reproduction system is provided using a computer network that comprises a server, at least one attachment unit that is coupled to the server and first and second reproduction devices. The server storing data to be reproduced. At least one attachment unit comprising means for interfacing with a portable memory device having a reference to the reproduction data. The first reproduction device capable of performing a first data reproduction of the reproduction data and the second reproduction device capable of performing a second data reproduction of the reproduction data, the second data reproduction being different than the first data reproduction. Wherein the server responds to a request from the at least one attachment unit by transmitting the reproduction data and where the reproduction data is determined to be a format unsuitable for the reproduction device, the data is reformatted for use by the reproduction device.

Abstract: A stent graft introducer for intraluminal deployment of a stent graft (26), the introducer comprising a stent graft release mechanism (6) to allow partial release of the stent graft (26) when carried on the introducer, whereby control of the stent graft can be maintained while allowing access into the lumen of the stent graft from at least one end of the stent graft. The partial release can comprise partial release of one end of the stent graft.

Abstract: An introduction arrangement for a fenestrated or branched stent graft (13) intended for deployment into the lumen of a vessel having a blind vessel extending from it. The introducer (1) has a distal end intended to remain outside a patient in use and a proximal end with a nose cone dilator (11) and an arrangement to retain the branched stent graft distally of the nose cone dilator. A sheath (15) on the introducer extends over the branched stent graft to the nose cone dilator. An indwelling catheter (22) extends from the distal end of the introducer and enters the fenestration or side arm and through to the nose cone dilator, the indwelling catheter has a guide wire (29) extending through it. The guide wire can be extended beyond the nose cone dilator in use before the sheath is withdrawn from the branched stent graft so that it can be snared from the contra-lateral artery.

Abstract: A modular endoluminal prosthesis includes a first prosthetic module (40) having an opening at one end (41) and an internal surface (46), and a second prosthetic module (50) having an opening at one end (43) and an external surface (48). The first and second modules (40, 50) are connected by inserting the one end (43) of the second module (50) into the one end (41) of the first module (40). Either the internal surface (46) or the external surface (48) comprises at least one projection (42 or 44) and the other of the internal surface or the external surface comprises at least one surface feature (42 or 44) which engages the at least one projection (42 or 44) when the modules (40, 50) are connected.

Abstract: A medical grasping device (10) for vascular use, having an outer sheath (12), an elongate control member (50) extending within an outer sheath (12) to a distal tip section (54), and a proximal control assembly (22) including an actuation section (24) joined to the elongate control member (50). Adjacent to the distal tip section (54) is a grasping portion (70,70?) that is extendable from the outer sheath (12) to create loops (74,74?) for grasping a target object (T) for repositioning within the vascular system, or for removal from the patient, with loops being retractable into the outer sheath to hold the target object against the device (10) during movement of the device. Elongate control member (50) is preferably a cannula or tube having a lumen (58) extending completely therethrough for placement over a guide wire (28) already in the patient.

Abstract: A medical grasping device (10) for vascular use, having an outer sheath (12), an elongate control member (50) extending within an outer sheath (12) to a distal tip section (54), and a proximal control assembly (22) including an actuation section (24) joined to the elongate control member (50). Adjacent to the distal tip section (54) is a grasping portion (70, 70′) that is extendable from the outer sheath (12) to create loops (74, 74′) for grasping a target object (T) for repositioning within the vascular system, or for removal from the patient, with loops being retractable into the outer sheath to hold the target object against the device (10) during movement of the device. Elongate control member (50) is preferably a cannula or tube having a lumen (58) extending completely therethrough for placement over a guide wire (28) already in the patient.