Abstract: Ablation of the pulmonary veins causes damage to the tissue which may affect the viability of the tissue. By placing a stent, a vascular endoprosthesis, within a target pulmonary vein it is possible to protect the functionality of the veins after the ablation procedure. Placement of a stent, endoprosthesis or mere circuit interrupting structure into a target pulmonary vein, without ablation, prevents aberrant electrical activity in the pulmonary veins from interfering with the electrical activity of the left atrium. The stent, endoprosthesis or circuit interrupting structure may also be coated or comprised of a drug-eluting compound, loaded with a drug which inhibits arrhythmia.

Abstract: The present invention is a synthetic, biocompatible, bioabsorbable, porous foam tissue scaffolds possessing physicochemical properties suitable for use in the repair and regeneration of dermal tissue and to methods of preparing the foam scaffold.

Abstract: A minimally invasive method of performing mitral annuloplasty is disclosed. An implantable device is positioned within the coronary sinus and tightened around the mitral annulus. Mitral valve regurgitation is monitored before, during, and/or after the tightening step. An on-going drug therapy may be determined, taking into account post-implantation hemodynamic function.

Abstract: A patellar bearing having extended, rounded contours on the superior and inferior edges of its articulating surface.

Abstract: A left ventricle restriction device is designed to be transvenously advanced and deployed within the coronary sinus and in some embodiments other coronary veins. The device places tension on adjacent structures, reducing the diameter and/or limiting diastolic expansion of the left ventricle. This may be beneficial for patients with dilated cardiomyopathy.

Abstract: A method and apparatus of making repairs with graft ligaments. In one form, the method for graft ligament reconstruction comprises (i) harvesting a graft ligament consisting entirely of soft tissue; (ii) compacting the graft ligament through compression so as to significantly reduce the cross-sectional area and increase the density of the collagen material of the graft ligament; and (iii) deploying the compressed graft ligament in the human body. In another form, the apparatus for graft ligament reconstruction comprises a graft ligament having a given diameter and a given cross-sectional area; and a compacting instrument having at least one surface to contact the graft ligament and to decrease the given cross-sectional area of the graft ligament to a reduced cross-sectional area, whereby the graft ligament with the decreased cross-sectional area may be positioned within a bone tunnel having a cross-sectional area smaller than the given cross-sectional area of the graft ligament in its original state.

Abstract: A method of positioning a main stent at a vessel bifurcation such that a side opening in the main stent is positioned at the ostium of a branch vessel, comprising: positioning a main guidewire in the main vessel such that a distal end of the main guidewire extends past the bifurcation; advancing a stent delivery system to a position proximate the bifurcation, the stent delivery system comprising a catheter with a flexible side sheath attached thereto, wherein the catheter is received over the main guidewire, and wherein the main stent is positioned over the catheter with the flexible side sheath positioned to pass through the interior of the main stent and out of the side opening in the main stent; advancing a branch guidewire through the flexible side sheath attached to the catheter and into the branch vessel; and subsequently, advancing the catheter over the main guidewire while advancing the flexible side sheath over the branch guidewire while viewing relative movement of a marker positioned on the flexibl

Abstract: Decellularized vascular prostheses that are resistant to thrombus occlusion and have a low level of immunogenicity and methods of making same are disclosed. The prostheses have high mechanical strength, resist aneurysm, rupture, and allow for secure surgical sutures while maintaining structural integrity. The vascular prostheses provided are blood vessels, valves or portions of vessels containing valves. There is also a method useful for coating synthetic vascular stents.

Abstract: A system and method for delivering and positioning a stent within a bifurcated body lumen includes a stent delivery system including a catheter, expansion device, a stent with a side hole disposed on the expansion device, and an ultrasound transducer disposed between the expansion device and the stent. The ultrasound transducer is configured for transmitting and receiving signals and for imaging of a body lumen so as to locate an ostium of a branch vessel and facilitate alignment of the stent side hole with the ostium.

Abstract: A method for making a curved implantable sheath includes placing a sheet of flexible material into engagement with a member having a curved surface having a desired configuration. The sheet and member are placed in a fixation solution so that the sheet assumes the configuration of the surface engaged thereby.

Abstract: A method of increasing the rate of expansion of tissue area and volume, either in vivo or in vitro, which comprises preparing a tissue for expansion and subjecting the tissue to stretching forces, wherein the stretching forces are alternatively increased and decreased to provide alternating periods of stretch and relax cycles.

Abstract: A lumbar intersomatic implant for insertion into the discal space between two adjacent vertebrae for reestablishing the anatomical intervertebral space, the implant being in the form of a generally rectangular cage having two sagittal walls interconnected by at least an anterior transverse wall and a posterior transverse wall, the walls defining between them an open volume for filling with bone. An “outer” one of the sagittal walls of the implant presents a top rim and a bottom rim each shaped to present at least one retention edge extending substantially in the sagittal plane, making insertion via a posterior path possible, and an outer face arranged to present a penetration assisting shape enabling the cage to be offset transversely to a locking position in the discal space, which position is obtained by the retention edge preventing the cage from being reversed transversely.

Abstract: A plastic jacket for affixing an artificial joint to a bone. The plastic jacket includes a body for contacting with the bone, an opening for receiving the artificial joint, which is formed with a predetermined shape at one end of the body, and an closed wall formed at another end of the body.

Abstract: A foldable intraocular lens for implantation in the eye includes an optic made of a highly pliable material and a pair of fixation members made of a material that is flexible, but more rigid than the optic. The fixation members are integral with a cantilevered arm that extends radially outward from the optic. Each fixation member includes a proximal end at the outer end of the cantilevered arm, a distal end, and a flex portion intermediate the proximal and distal ends. The flex portions of the two fixation member extend generally away from one other adjacent their respective proximal ends on diametrically-opposed sides of the optic.

Abstract: This application provides a novel unitary bone implant having at least one rigid, mineralized bone segment, which may be machined to include threads, grooves, a driver head, perforations, a recess, or a symmetric shape, and a flexible, demineralized segment, which may also be machined to any desired shape prior to demineralization, or after demineralization. The disclosed implant has wide orthopedic applicability, including but not limited to repair or replacement of ligaments, tendons, and joints and for inducing vertebral fusions and fractured bone repair.

Abstract: A bioabsorbable implantable endoprosthesis having elongate elements including hollow, cavity or porous portions adapted to accumulate by-product from the degradation of the bioabsorbable material and shortening the diffusion distance for water absorption and thereby relatively increasing the degradation of the structure.

Abstract: A system for repairing body lumens including a modular graft and a method for deploying the graft within the body lumen. The modular graft includes a first component having first and second legs portions which mate with second and third graft components, respectively. The second leg portion has a bell bottom shape. The modular graft further includes expandable members which aid in implanting the modular graft as well as facilitates the mating of its components. In order to repair the body lumen, the first component is placed at the repair site and thereafter the first and second legs are advanced to the repair site and attached to the first component. A further aspect of the invention is a fixation device which is adapted to perform an attachment function. The graft and the fixation device are configured to be axially separated from one another so as to allow the graft to attach to the vascular wall proximal of the graft.

Abstract: A medical device delivery apparatus is provided which comprises a catheter having an expandable and contractible member and an expandable medical device disposed about the expandable and contractible member. At least portions of at least one of the medical device and the expandable and contractible member have a pressure sensitive adhesive applied thereto to adhere the medical device to the expandable and contractible member. The pressure sensitive adhesive is selected so as to release the medical device from the expandable and contractible member upon contraction of the member from an expanded state. Suitable medical devices include stents.

Abstract: A device to provide body fluid flow control in the form of a valve to be located within a duct or passageway. The device is controlled through pressure above a preselected threshold. Bulk resilience about a passageway in a valve body provides the mechanism for controlled flow. One-way valve operation may be provided through a flap or through a pressure differential on the valve body depending upon the direction of flow. A frame structure positioned within a resilient seal includes longitudinally elongate elements which may be of spring material, malleable material or heat recoverable material so as to accomplish an initial insertion state and an expanded anchoring state. A valve support transitions between the resilient seal portion and the valve body to insure that the states do not change the threshold opening pressure. Insertion devices may be employed to position and actuate a change of state of the frame in the body duct or passageway.

Abstract: A catheter assembly for delivering an endoprosthesis within a body lumen. A delivery catheter assembly is provided which includes a stent with biocompatible material thereon for preventing the stent from expanding or otherwise dislodging from the catheter. The stent with biocompatible material is secured to an expandable member of a delivery catheter, whereby inflation of the expandable member causes the biocompatible material to fail, thereby permitting the stent to expand and deploy in a body lumen.