Abstract: An expandable, bistable open cell design incorporates the following features: a first relatively stiff portion (152) having first and second ends and a first relatively flexible portion (154) connected to the first and second ends of the first relatively stiff portion, the first relatively stiff portion and the first relatively flexible portion substantially surrounding a first open area (156) of the stent structure; a second relatively stiff portion (158) having first and second ends and a second relatively flexible portion (160) connected to the first and second ends of the first relatively stiff portion, the first relatively stiff portion and the first relatively flexible portion substantially surrounding a second open area (162) of the stent structure; and an opening (110) formed through the first relatively stiff portion and the second relatively flexible portion such that the opening connects the first and second open areas, thereby creating first and second intermediate ends (152a, 152b) of the first r

Abstract: A device for performing examination through the uterine cavity, preferably to carry out a computed tomography virtual hysterosalpingography, by the use of a speculum and a cannula or probe, wherein the device comprises a support for centering in the speculum and the probe is retained in a central end of the support to guarantee the centering of the probe within the cervix and the holding of the probe in the desired position during the test.

Abstract: An endoluminal prosthesis system includes a tubular graft having a pocket on the exterior of the graft. The graft further includes a wire extending within a lumen of the graft, with the wire extending through the passageway and into the pocket. An extension prosthesis can be inserted over the wire and into engagement with the pocket and the passageway, where the extension prosthesis can be sealed with the pocket and the passageway to seal the otherwise unused passageway in the graft.

Abstract: A method for performing an annuloplasty includes positioning an annuloplasty ring structure along an atrial surface of an annulus of a heart valve. While a distal portion of a tube is longitudinally advanced through a channel of the ring structure, it faces a first portion of tissue of the annulus. A first tissue anchor is anchored to the first portion of tissue, from within the channel, while the distal end of the tube faces the first portion of the tissue. After moving the distal portion of the tube to a second portion of the structure, the second portion of the structure is anchored to a second portion of tissue by anchoring a second tissue anchor to the second portion of the tissue while the distal end of the tube faces the second portion of the tissue. Other embodiments are also described.

Abstract: A medical device for treating hip joint osteoarthritis in a human patient is provided, the hip joint comprises an acetabulum, being a part of the pelvic bone, and a caput femur, being connected to the collum femur and being the upper extremity of the femoral bone. The caput femur and collum femur further comprises cortical bone, the outer more sclerotic bone, and cancellous bone, placed in the bone marrow, said medical device comprising: an artificial caput femur surface, adapted to be in contact with the acetabulum surface or an artificial replacement therefor, and a fixating member adapted to at least partly be stabilized by the cortical bone of a stabilizing part of the collum femur.

Abstract: The invention provides an improved stent design for repairing vasculature, the stent having rings including struts defining first peaks and second peaks, selected second peaks of adjacent rings being connected by links. The stent design incorporates non-linear links with undulating portions extending generally perpendicular to or circumferentially with respect to a longitudinal axis of the stent and adjacent first peaks with different longitudinal lengths such that stent flexibility is increased without sacrificing stent compression for delivery.

Abstract: Apparatus for repairing a shoulder joint, including a baseplate having a base portion having a medially-facing surface and a laterally-facing surface, and an opening passing through the medially-facing and laterally-facing surfaces for receiving a screw; and an anterior flange having an anteriorly-facing surface and a posteriorly-facing surface, the anterior flange extending away from, and perpendicular to, the medially-facing surface, the anterior flange having an opening passing through the anteriorly-facing and posteriorly-facing surfaces for accepting a screw; an articulating surface component for mounting to the laterally-facing surface for covering the laterally-facing surface; and an anterior cover for mounting to the anteriorly-facing surface and configured to lock the articulating surface component to the base portion, such that when the anterior cover is mounted to the anterior flange, the articulating surface component is locked to the base portion.

Abstract: The invention relates to a structure having fibers which are adhesively bonded to one another in locations and have a permeability for air of between 0.5 ml/min*cm2 and 1.5 ml/min*cm2, wherein said structure has an at least one-sided coating which reduces the permeability of the structure to below 0.2 ml/min*cm2.

Abstract: An acetabular cup prosthesis comprising an acetabular cup having a rim and comprising a metal band applied around the outer circumference of the acetabular cup prosthesis and adjacent to said rim.

Abstract: Stents or scaffolds made from magnesium or magnesium alloys including additives or barrier coatings that modify the corrosion rate of the stent are disclosed. Methods of forming barrier coatings that modify the corrosion rate of the stent are disclosed.

Abstract: An implantable medical device includes a frame that includes at least one elongate member. The implantable medical device also includes a fixation member that has a first cuff, a second cuff, a tissue engagement member configured to anchor to tissue at an implant site to thereby hold the implantable medical device in a position at the implant site, and a cuff joining member that has an arcuate shape and that is connected at a first end to the first cuff and at a second end to the second cuff. The first cuff substantially surrounds a perimeter of a first portion of the at least one elongate member, the second cuff substantially surrounds a perimeter of a second portion of the at least one elongate member, and the cuff joining member does not substantially surround a perimeter of any portion of the at least one elongate member.

Abstract: A prosthetic heart valve includes a collapsible and expandable stent having a proximal end, a distal end, an annulus section adjacent the proximal end and an aortic section adjacent the distal end. The stent is formed of a plurality of struts. A cuff is coupled to the stent. The cuff has one or more features configured to reduce abrasion and/or perivalvular leakage.

Abstract: The present teachings are directed to a shoulder prosthesis having an adjustable radial offset and/or angular inclination provided by relative rotation of an adapter interdisposed between a stem and a head. In one example, a prosthesis has a stem having a first longitudinal axis. The prosthesis can also include an adaptor including a first taper. The first taper can have a first taper axis. The prosthesis can include a head supported by the adaptor. The head can be selectively oriented and then coupled to the first taper and the combination can be selectively orientated and the coupled to the stem.

Abstract: An orthopedic system prepares a surface of an anatomical structure to receive an orthopedic prosthesis. A method for using the same is also disclosed. The orthopedic system includes a surgical instrument and a guide. The guide includes an anterior portion and a distal portion that is at least partially elevated relative to the anterior portion. The distal portion includes at least one track that is sized to receive the surgical instrument while preparing the surface of the anatomical structure.

Abstract: Cruciate ligament substitutes are formed using fan-folded iliotibial band grafts of fascia lata. Devices of making the same and methods of making and using the same are described herein. The thick fan-folded grafts of fascia lata cruciate ligament substitutes disclosed herein are used in a single-loop fashion and have surprisingly exhibited load to failure and stiffness values that compare favorably with conventional grafts, including tibialis anterior, tibialis posterior, peroneus longus, and bone-patellar tendon-bone (BPTB) half-patella specimens, when the harvested iliotibial band grafts of fascia lata avoid portions thicker than 5 mm, or even 3 mm.

Abstract: A method and apparatus for fixing a ligament in a bone tunnel by cross-pinning the ligament in the bone tunnel.

Abstract: A prosthesis and a method of manufacturing the prosthesis for controlling flow through a bodily lumen are provided. The prosthesis includes a body having a proximal portion, a distal portion and a lumen extending therethrough. The prosthesis also includes a valve operably connected to the body. The valve has a proximal portion, a distal portion and a lumen extending through the valve, where the valve lumen is connected to the body lumen. The valve is configured to be closed in the absence of an antegrade pressure and a retrograde pressure, the retrograde pressure being greater than the antegrade pressure. The valve includes a material portion operably connected to the valve, the material portion providing increased stiffness to the valve relative to the valve alone, wherein the material portion is configured to facilitate self-reversion of the valve to the closed configuration.

Abstract: A surgical tool includes a shaft for receiving implants. The shaft defines a non-linear track. The tool includes a deployment member movable along the track to deploy the implants. An implant includes a body, and a plurality of alternating threads and flutes helically arranged about the body such that the body rotates under a linear applied force. Alternatively, an implant includes a body having a distal end for pound-in advancement into tissue. The body includes a plurality of cone-shaped, stacked barbs. A surgical tool includes two implants. The first implant has forward threads and the second implant has reverse threads. The first implant has threads for rotary advancement into tissue and the second implant is configured for pound-in advancement into tissue. The first and second implants are configured for pound-in advancement into tissue.

Abstract: An orthopaedic knee prosthesis includes a femoral component which exhibits enhanced articular features, minimizes removal of healthy bone stock from the distal femur, and minimizes the impact of the prosthesis on adjacent soft tissues of the knee.

Abstract: A tool and method for locating a proper position for a portal incision for hip arthroplasty, the tool having at least one generally straight body defining an axis, the generally straight body having a slot at one end, the slot being angled at an approximately 45 degree angle relative to the axis of the generally straight body, the slot configured to receive a cutting member or guide tool. A second generally straight body may be connected to the first generally straight body to form a right angle. If the lengths of the two generally straight bodies are substantially equivalent, then when the second generally straight body is inserted into the acetabulum, the first generally straight body positions the slot in the proper location such that sliding a guide tool or cutting member through the slot allows a portal incision to be created in the proper location. In some embodiments, the generally straight bodies may have adjustable lengths.