Abstract: A medical device includes an elongated member and a reinforced retention structure. The device can be used for draining substances from organs or abscessed areas within a body of a patient. The elongated member is made of a flexible material. The reinforced retention structure extends from or is formed integrally with the elongated member and comprises an elastic member and the flexible material. The reinforced retention structure provides retention strength while providing flexibility and patient comfort. The use of the reinforced retention structure also provides increased stability to the device within the patient's body and combats migration and/or expulsion of the device. The nature of the reinforcement in the retention structure may extend into the elongated member, which allows for larger drainage openings in the device and increases the radiopacity of the device.

Abstract: A method of performing a medical procedure is disclosed which involves the use of a balloon catheter in combination with an angioscope to monitor an intravascular stent before, during or after deploying the stent. Specifically, the method may include the steps of (1) delivering an intravascular stent into the vasculature of a patient, (2) positioning a balloon catheter in the vasculature such that the inflatable balloon is adjacent the stent, (3) inserting an angioscope into the balloon catheter such that the distal end of the angioscope is adjacent an optically-transparent tube traversing the interior of the balloon, and (4) visually monitoring the stent before, during or after deploying the intravascular stent. The optically-transparent tube may define a guide wire lumen for use with a guide wire and the angioscope may be inserted into the guide wire lumen. The intravascular stent may be a balloon-expandable stent, a self-expanding stent, or a stent made of a photo-responsive polymer.

Abstract: A robotic surgery apparatus comprising: a surgical instrument for use at an internal operative site of a subject; a mechanically drivable mounting unit on which the surgical instrument is mounted, the mounting unit being drivably movable outside the operative site of the subject; an electrically driven drive unit for driving movement of the mounting unit; mechanical cabling drivably intercoupled to the mounting unit at one end of the cabling; the mechanical cabling having another end which is readily drivably couplable to and decouplable from the drive unit. The drive unit being readily manually portable and readily attachable to and detachable from a fixed support on or relative to which the subject is mounted.

Abstract: An apparatus for treating a biological tissue of a patient in situ includes an optical fiber for guiding a coherent waveform of a selected wavelength to a fiber tip. The wavelength is selected to have a low absorption in water. The fiber tip is contained within a guide member having a discharge bore to define an unobstructed light pathway. The guide member is adapted to be slidable along a tissue surface in atraumatic sliding engagement with the discharge bore opposing the surface. The guide member is carried on an elongated flexible member.

Abstract: An electrosurgical probe comprises a shaft having at least one electrode terminal at its distal end and a connector at its proximal end. The electrode terminal may be spaced from a return electrode such that when the electrode terminal is brought adjacent a tissue structure immersed in an electrically conductive fluid from outside the body, the electrically conductive fluid completes a conduction path between the electrode terminal and the return electrode. By applying high frequency electrical energy to the electrode terminal, target tissue may be cut or ablated while heat dissipation through low impedance paths, such as blood and normal saline, will be minimized. Related methods are disclosed.

Abstract: The present invention provides an apparatus and a method for producing a virtual electrode within or upon a tissue to be treated with radio frequency alternating electric current, such tissues including but not limited to liver, lung, cardiac, prostate, breast, and vascular tissues and neoplasms. An apparatus in accord with the present invention includes a supply of a conductive or electrolytic fluid to be provided to the patient, an alternating current generator, and a processor for creating, maintaining, and controlling the ablation process by the interstitial or surficial delivery of the fluid to a tissue and the delivery of electric power to the tissue via the virtual electrode.

Abstract: An electrosurgical return electrode for use in electrosurgery. The return electrode is self-limiting and self-regulating as to maximum current and temperature rise to prevent patient trauma. An inductor is coupled in series with the return electrode. The inductor counteracts at least a portion of the impedance of the return electrode and the patient to optimize the flow of the current when the amount of contact area between the patient and the return electrode is sufficient to perform electrosurgery. The inductor may also be variable to allow the overall impedance of the electrosurgical circuit to be adjusted and tuned to work properly and safely with a particular patient and the other equipment used to perform electrosurgery. A conductor member operates with circuitry that indicates to a user when the contact area between the patient and the self-limiting member and/or return electrode is below a given threshold.

Abstract: An electrosurgical instrument that allows precise modulation of active Rf density in an engaged tissue volume. The working end of the instrument has a tissue-contacting surface of a conductive-resistive matrix that is variably resistive depending on its temperature. The matrix comprises a positive temperature coefficient (PTC) polymeric material hat exhibits very large increases in resistivity as any local portion increases beyond a selected temperature. In a method of use, the polymeric PTC material senses the temperature of engaged tissue in a manner akin to pixel-by-pixel sensing and thereby changes its resistance in a corresponding pixel-by-pixel manner. The instrument further carries cooling means to cause accelerated thermal relaxation of the PTC matrix during use to make the engagement surface highly responsive to temperature changes that in turn alter the matrix between being electrically conductive and electrically resistive.

Abstract: A ureter resectoscope with an elongate flexible stem tube (4) of substantial length and small external diameter, of which the distal end piece (5) is made from insulating material and which accommodates an optical unit (6) as well as a rod-shaped instrument carrier (11). The instrument carrier is disposed so as to be longitudinally displaceable parallel to the optical unit and bears on its distal end an electrode (12, 12?) that can be supplied with high-frequency current and, on its proximal end after passing through a bore in a main body (1) disposed on the proximal end of the stem tube, is fixed and electrically contacted on a slider (13) mounted so as to longitudinally displaceable.

Abstract: A suction cautery dissector comprising a handle assembly, a tubing assembly having a suction channel formed therein, the tubing assembly comprising a first portion connected to the handle assembly and a distal end, and a tip assembly at the distal end of the insulated tubing assembly, the tip assembly comprising a substantially co-planar, enclosed cautery surface with a beveled leading edge sharpened for dissecting tissue. The cautery surface provides an opening formed therein that communicates with the suction channel in the insulated tubing assembly and being operably connected to an electrical source.

Abstract: A device for external fixation of a fracture of the proximal end of the ulna includes an frame having a distal elongated portion extending below the ulna, holding a number of pins extending upward into the shaft portion, and a proximal portion extending rearward, and upward around the proximal end of the ulna, holding a medullar pin extending into a medullar channel and a number of pins extending into fragments of the fractured ulna.

Abstract: A spinal plate comprises a body portion and at least one locking mechanism for engaging the body portion. The body portion is made of a radiolucent material, such as a polymer or polyether ether ketone (PEEK), and includes a plurality of bone screw openings for receiving a plurality of bone screws, such as bone screws. The at least one locking mechanism is for securing at least one of the plurality of bone screws when received into the body portion.

Abstract: A method of stimulating bone regeneration in a discontinuous section of a long bone in a subject requiring same, comprising the step of applying to said discontinuous section of the bone an effective vacuum for an effective length of time. A device for carrying out the method consisting of a sealable tubular-shaped sleeve or cuff that fits snugly and sealably around the bone section to be treated and that can be evacuated via a port that is integral to the sleeve or port.

Abstract: This invention relates to methods and instruments for performing a surgical procedure in a disc space between adjacent vertebrae. The instruments include a distractor and a cutting instrument. In one embodiment the distractor includes a body portion and a pair of flanges extending along opposite sides of the body portion such that a slot is formed between the flanges and the body portion. The cutting instrument is positionable over the body portion and into the slots of the distractor so that the flanges are positioned between the cutting instrument and the adjacent tissue.

Abstract: Surgical instrument for inserting an intervertebral prosthesis, having first and second prosthesis holders (52A, 52B) for a pair of prosthesis plates, which holders are connected to one another by a parallel guide (57) and can be spread by a lever arrangement (131). The first of the prosthesis holders is arranged on an elongate instrument body in order to give the surgeon an exact picture of the orientation of the prosthesis and to allow force to be exerted in exactly this direction. The actuating lever (131) is articulated with its front end on the second prosthesis holder (52B) so as to pivot about a spindle (130) extending transversely with respect to the longitudinal direction of the instrument body (51) and to the direction of spreading. Behind this spindle (130), it has a limit stop (133) which acts directly or indirectly on the instrument body (51) or the first prosthesis holder (52A). The lever arrangement can also be the other way around.

Abstract: A medical retrieval device includes a basket formed of two or more loops. The basket may be used to retrieve material (e.g., a urinary stone) from a body. The basket opens and closes for end-encapsulation of a stone and is strengthened by support members that interconnect the basket loops. A captured stone may be released from the basket with the basket still in the body by opening the loops.

Abstract: A needle is guided to a target along a pre-determined needle insertion trajectory. A method that utilizes a fluoroscope can be used to locate the target. The target can be an internal structure within the human body. A device can be used with the fluoroscope to aim and insert a needle or sharp probe along the predetermined trajectory to the target. By using the device with the fluoroscope, a user can receive real time visual confirmation of contact between the needle and the target.

Abstract: A device for snaring cord-like objects is provided. The device comprises a hollow shaft having a pointed distal end, a rod having a pair of wires attached to its distal end, the wires being spring biased away from one another, and activation means. The rod and wires are located in the lumen of the shaft in reciprocally movable relationship therewith. The activation means is attached to the proximal ends of the shaft and the rod so as to allow the controlled movement of the rod and wires relative to the shaft. One of the wire-like elements defines a hook-shaped configuration at its distal end. The device allows the wire-like elements to be selectively located within the distal end of the shaft or in a configuration wherein the wire-like elements extend outwardly from the distal end of the shaft in flaring relationship to one another.

Abstract: A surgical tacking apparatus for forming and applying surgical fasteners during laparoscopic or endoscopic procedures is disclosed. It includes a housing having a handle, an elongated tubular portion extending from the housing, a wire advancer, and a wire shaping nose at its distal end. An annular fastener is also disclosed.

Abstract: A tissue retaining ring for use with a plurality of surgical fasteners mounted within a disposable loading unit utilized during a vascular anastomosis inlcudes a genrally circular, semi-pliable material having a series of alternating loops and arcuate portions. Each of the loops defines an aperture therein which is dimensioned to receive a distal end of one of the plurality of surgical fasteners. When the instrument is fired, the surgical fasteners are simultaneously deformed through the tissue ring and through the tissue. The tissue retaining ring holds the tissue in place along the surgical fastener and reduces the chances of tissue slippage after deformation.

Abstract: A safety trocar is provided in which the cannula is reciprocally mounted to the cannula housing and reciprocates into the cannula housing when a proximally directed force is applied thereto. The piercing tip is maintained in the exposed position by a latching mechanism associated with the obturator shaft, and is automatically withdrawn into the cannula under the force of a spring when the proximal force is removed from the cannula, the cannula thus advancing distally and releasing the latching mechanism. Penetration force is maintained at a minimum, and safe and efficacious trocar entry is facilitated.

Abstract: The present invention is directed to an apparatus for anchoring a tubular element, preferably in the form of a catheter, within a passageway formed in a mammalian body, such as in a vessel, artery, duct, channel, or the like. The apparatus comprises a tubular element having a flexible, elongated, hollow tubular outer lumen with a central longitudinal axis extending therethrough, the outer lumen having a proximal end and a distal end. The apparatus further comprises deployment means positioned within the outer lumen and slidable with respect to the outer lumen. The deployment means has a proximal end and a distal end. The apparatus further comprises a plurality of resilient anchoring members preferably formed of a pseudoelastic material. The anchoring members are coupled to the distal end of the deployment means and extend longitudinally beyond the distal end of the deployment means. Each anchoring member is reversibly movable by the deployment means between a first position and a second position.

Abstract: A tubular guidewire assembly having a distal occlusive device and an extended crimpable section proximate a proximal end that is adapted to connect to a gas inflation/evacuation system. The extended crimpable section can be selectively sealed at one of a plurality of separate locations to form an airtight seal of the tubular guidewire assembly. Each time a deflation of the occlusive device is desired in order to reestablish blood flow to a vessel downstream of the occlusive device, the extended crimpable section preferably is cut distal to the location of the last seal to quickly deflate the occlusive device.

Abstract: A balloon catheter comprises a shaft including a tubular having a relatively rigid proximal shaft section and a distal shaft section, each section connected to one another through a flexible transition member, and an inflatable balloon extending at a distal portion of the distal shaft section. The proximal and distal shaft sections define an inflation lumen extending therein which is in fluid communication with an interior of the balloon to allow inflation pressure to the balloon. The distal shaft further comprises a guide wire lumen to receive a guide wire. The guide wire lumen has a guide wire inlet, located between the end portion of the proximal shaft section and the balloon, and a guide wire outlet, located distally to the balloon and leading to an exterior of the catheter. The balloon catheter can be used for coronary angioplasty.

Abstract: A balloon catheter for treatment of a patient's lacrimal system is applied transnasally without the use of a guide wire or a curve retention member. The catheter uses a stainless steel hypotube of sufficient stiffness and column strength to be pushed from the patent's nasal cavity through an opening-formed through the lateral nasal wall and lacrimal fossa, into the lacrimal sac. The catheter has an inflatable member mounted about a rigid bent distal segment. The opening is first formed by pushing small holes through the medial sac, lacrimal fossa, and lateral nasal wall with an instrument and coalescing the holes. The catheter is then introduced into the nasal cavity and pushed laterally through the opening by manipulating its proximal end. Pressurized fluid is then applied to the catheter to inflate the inflatable member and dilate the opening.

Abstract: The invention provides a delivery system for placing devices in atrial appendages. The system includes a catheterization apparatus having a tubular structure with one or more nested tubes, wires, and shafts. The tubes establish a passageway for moving a device through a body's vasculature and heart into an atrial appendage. An expandable positioning guide is disposed on the distal end of a tube passing through the apparatus. The positioning guide is expanded in situ to engage atrial wall surfaces proximate to the atrial appendage for mechanical support. The deployed positioning guide mechanically stabilizes the device delivery passageway. A shaft passing through the tubes transports the device through the passageway to the atrial appendage. The system includes catheterization apparatus for transseptal delivery of the devices. An outer tube or sheath in the apparatus is used to penetrate and traverse the septum. An expandable securement device is disposed toward an end of the sheath.

Abstract: A rapid exchange sheath comprising an elongate tubular member, a guidewire, and support wire having an expandable filter at a distal end. The guidewire passes through a first opening at a distal end of the tubular member and a second opening a short distance proximal from the distal end. The support wire is received in a lumen of the tubular member, or, in certain embodiments, extends proximally through a third opening a short distance proximal from the distal end. Methods of using the sheaths for deploying and/or exchanging medical device(s) in a patient's vessel are also disclosed.

Abstract: Apparatus for collecting emboli flowing in a lumen. A motor has a longitudinal bore, a friction area within the longitudinal bore, and a guide wire disposed within the longitudinal bore. The guide wire and friction area of the motor are sized and adapted to contact each other and impart friction between the friction area and the guide wire to permit the motor to rotate around the guide wire. A thrombus collecting gutter is attached to the motor. Paddles are attached to motor and are adapted to initiate a spiral blood flow when the motor rotates. The spiral blood flow causes thrombii in the blood to be deflected towards the internal wall of the lumen and be trapped in a thrombus collecting gutter which is positioned on the motor downstream of the paddles.

Abstract: The present invention is directed to a medical device, such as an endoscopic device, configured to be loaded into a channel of an endoscope prior to insertion of the endoscope into a body, and a method of performing an operative procedure with an endoscopic device. The endoscopic device comprises an elongate member for insertion into the channel of the endoscope, wherein a length of the elongate member is greater than a length of the channel of the endoscope. The endoscopic device also comprises a distal assembly connected to a distal portion of the elongate member and operable to perform an endoscopic operation, wherein the distal assembly has an open configuration and a closed configuration with a profile larger than a diameter of the channel of the endoscope, wherein the distal assembly is adapted to be exterior to the channel when the endoscope is inserted into the body.

Abstract: A percutaneously insertable system for sealing punctures in blood vessels includes an element that is percutaneously insertable into and deplorable within a blood vessel, a thread-like member attached to the element that passes through the wall of the blood vessel and arresting element movable on the thread and into engagement with the other surface of the blood vessel thereby to seal the opening.

Abstract: A force-transmitting head for a chiropractic adjustor apparatus includes a hub which is rotatable in a cavity formed in the head and non-rotatably attached to a reciprocating shaft of the apparatus. A rotation pin extends through the body into the cavity and engages a track formed in the hub. Reciprocating movement of the shaft and hub causes a rotational movement of the body with passage of the rotation pin along the track. Also, a chiropractic adjustor apparatus incorporating the force-transmitting head.

Abstract: A self-expanding stent delivery apparatus having a sheath comprising a hard and lubricious coating for the safe, effective and accurate deployment of self-expanding stents. The sheath comprises an inner layer of pyrolytic carbon or other similar substance which prevents the stent from becoming embedded. The inner layer is also lubricious. This combination of properties allows for easier deployment and reduced profile.

Abstract: A system for performing a medical treatment in a blood vessel while providing downstream microcirculatory system protection, the system being composed of: a catheter having a longitudinal axis, a distal end, an outer lateral surface, a central blood bypass flow lumen extending along the longitudinal axis and opening at the distal end, blood flow inlet and outlet openings extending from the lateral surface and communicating with the bypass flow lumen, and first and second inflation lumens extending to the lateral surface at respective first and second locations that are spaced apart along the longitudinal axis and that are between the inlet openings and the outlet openings; and first and second inflatable members secured to the lateral surface and each having an interior that communicates with a respective one of the first and second inflation lumens, wherein the catheter has a thin outer wall enclosing a hollow interior that is completely occupied by the bypass flow lumen, except for the space occupied by the

Abstract: A method and apparatus for caged stent delivery is provided herein. The device can be used to position and deliver any type of stent to a preselected treatment site within an intraluminal cavity. The device comprises a tubular portion, a plurality of arms attached to the distal end of the tubular portion, and a mechanism to open the arms. In operation, the caged device carries a stent in a constricted form to the treatment site for deployment. The arms of the cage are then opened, the stent released and deployed, and the device withdrawn. Several methods are provided to open the arms, including various pullwires, a piston, an electrolytic joint, and an activator. The arms may be constructed of a shape memory alloy and opened when shape memory behavior is effected. The device may be used with conventional catheters or used with a stent-loaded guidewire.

Abstract: A composite stent and a method for making the same are provided.

Abstract: The present device has increased longitudinal flexibility in a stent by having some curved sections of each circumferential set of strut members being unconnected to the curved sections of the adjacent circumferential set of strut members with the other curved sections being connected by highly flexible, undulating longitudinal connecting links. The present device prevents flaring of the unconnected strut members by having a shorter longitudinal length for the unconnected strut members, and may have generally shorter longitudinal lengths for all the strut members in the circumferential sets of strut members at the stent ends to reduce the tendency for end flaring of the stent. Finally, the stent demonstrates that the flexible longitudinal connecting links of the curved sections of the sets of strut members are connected at a point that is close to the line where the diagonal sections join the curved sections, thus further reducing the propensity for end flaring.

Abstract: The stent of this invention is a self-expanding stent created by a scaffolding lattice. The stent may be made from a nickel-titanium alloy. The lattice is formed from two different types of helices that proceed circumferentially in opposite directions along the longitudinal axis of the stent. The helices have no free ends. The first type of helix is formed by a series of undulations and the second type of helix is formed from a series of connection elements. The undulations may be in a zigzag or sinusoidal pattern. The connection elements connect the junction points lying on adjacent turns of the first type of helix. The junction points are formed by the ascending and descending arms of the undulations or zigzags. The ends of the stent may be formed by a closed circumferential element which is linked by connection elements to a transition zone. The transition zone is formed by a closed loop that connects directly to the first helix.

Abstract: A prosthesis that resiliently engages a body passage includes an annular clamping ring which may be folded along a diametric axis for insertion into the body passage. The clamping ring is adapted to resiliently spring outwardly, once in position inside the body passage, and to be continually resiliently biased against the interior surface of the body passage. One or more of the clamping rings may be attached to opposed ends of a tubular graft. The rings and connected graft may be positioned in the body passage using an applicator which selectively permits expansion and/or in some embodiments contraction of the annular ring in position within a body passage. Alternatively a retaining member may be used to retain the annular ring in a compressed condition until it is in a desired position within a body passage. Among other potential uses, the present invention may be useful as a vascular stent for treating abdominal aortic aneurysms.

Abstract: A bifurcated stent comprises a body portion, a first branch portion, a second branch portion, a first pivot portion and a second pivot portion constructed from a common continuous sheet of stent material. The body portion, first branch portion and second branch portion provided with a substantially tubular shape, the tubular shape of each defines a lumen respectively therethrough. The lumen defined by the body portion is in fluid communication with the lumen defined by the first branch portion and the second branch portion. The first branch portion is pivotally engaged to an end of the body portion by the first pivot portion. The second branch portion is pivotally engaged to an end of the body portion by the second pivot portion.

Abstract: Coatings for stents that include a polymer and a drug are provided. A method of forming the coatings is also provided.

Abstract: A drug delivery device is provided with openings for directional delivery of a plurality of therapeutic agents to blood vessels or other lumens or organs. In particular, the invention relates to the delivery of different therapeutic agents, different quantities of therapeutic agents, or different release profiles of the same or different therapeutic agents in different directions from the drug delivery device. The invention is useful, for example, for delivering antirestenotic, antithrombotic, antiplatelet, antiproliferative, antineoplastic, immunosuppressive, angiogenic, anti-inflammatory, or antiangiogenic agents and/or vasodilators to a blood vessel. In one embodiment, antiproliferative, antineoplastic, angiogenic, antiangiogenic, anti-inflammatory, and/or antirestenotic agents are delivered to the wall of a blood vessel and antithrombotic agents, antiplatelet agents, and/or vasodilators are delivered to the lumen of a blood vessel.

Abstract: A system for breast augmentation includes a plurality of microballoons. An injector can be provided for injecting microballoons into a breast through an incision in the breast. The microballoons can have a first dimension when in the injector and a second, larger dimension when in the breast. An injector and tissue dissector are also disclosed. A method for performing breast augmentation surgery and microballoons for use in the method are also disclosed.

Abstract: An artificial disc to replace a damaged spinal disc in a spinal column includes an upper retaining member having an outer surface engageable with a first vertebra of the spinal column and an inner surface. A lower retaining member has an outer surface engageable with a second vertebra of the spinal column and an inner surface. A resilient core interconnects the upper and lower retaining members. The resilient core has an upper surface affixed to the inner surface of the upper retaining member. The resilient core has a lower surface affixed to the inner surface of the lower retaining member. The resilient core has a surface extending from one of the upper and lower surfaces toward another of the upper and lower surfaces and at least partially defining an empty space extending from the one of the upper and lower surfaces.

Abstract: Instrumentation for implanting an artificial intervertebral disc includes static trials and a dynamic trial for determining the appropriate size of disc to be implanted, a static trial holder for manipulating the static trials, an inserter/impactor for inserting and removing the static trials and for inserting the artificial intervertebral discs, repositioners/extractors for repositioning and extracting the static trials or the artificial intervertebral discs, and a leveler for setting the proper position of the artificial intervertebral disc.

Abstract: This invention provides a vertebral implant for impaction in a disc space to restore and/or maintain desired disc space height and spinal orientation. The implant has an elongated basis body having a generally lens-shape provided by convex upper and lower surfaces. Bearing surfaces are provided on the cross-edge surfaces of the endwalls. Grooves are provided in the upper and lower surfaces positioned between the bearing surfaces. The implant can be prepared from a wide variety of materials including metallic materials, synthetic materials, polymeric materials, ceramic materials, and composite materials including reinforced materials i.e. glass, fiber, and/or carbon fiber reinforced materials (CFRP). These preferred materials for fabricating implants in the present invention reduce costs, increase service life and provide excellent physiological compatibility. The non-metallic material can be selected to be either a substantially permanent material, a biodegradable material or a bioerodable material.

Abstract: Inverse prosthesis of the shoulder for the articulation of a humerus in a scapula of a shoulder comprising a glenoid cavity. The prosthesis includes an at least partly convex articulation element, including elements for support and attachment to the glenoid cavity, and able to articulate with an at least partly concave mating articulation element, associated with the top of the humerus. The articulation element includes a substantially hemi-spherical element and a pin-type implant element made as distinct and reciprocally removable elements, so as to allow them to be assembled sequentially with respect to the glenoid cavity.

Abstract: A plurality of canine acetabular cups designed to fit within different sized spherical reamed bone cavities to produce controlled interference without use of cements, screws or nails. Each of the canine acetabular cups, regardless of size, mates with a common femoral head, providing interchangeability. The controlled interference is obtained through use of a multiple curvature Ti—Al—V shell having a porous coating. The interference starts from zero at 50 degrees from the apex of the shell and extends to full interference value at 90 degrees from the apex. The Ti—Al—V shell carries a UHMW polyethylene insert, which is locked by interference, a non-circular post mated with an elongated opening and a circumferential locking groove mated with an interior projection. Initial stability is provided immediately after surgery due to the interference arrangement; long term stability is afforded by bone ingrowth.

Abstract: The present invention provides monopolar acetabular liners that can enclose a femoral head to form a hip replacement prosthesis, wherein the liner has a rim that creates an orifice, wherein the orifice has a diameter that is smaller than the diameter of the femoral head, and wherein the liner encompasses greater than 50 percent of the volume of the head, wherein a constraining ring can be used in conjunction with the monopolar constrained acetabular liner to provide additional support for the femoral head to stay with the acetabular liner and avoid dislocation. Assemblies, complete prosthetic replacements, and methods of replacing also are provided. Liners and constraining rings having no, one or more recesses also are provided.

Abstract: The present invention is directed to stents that are formed into a helical structure having a plurality of coils, a longitudinal axis, an internal longitudinal passage, a distal section and a proximal section having different diameters; where the structure is made from a fiber having a cross-section and including an inner core having an exterior surface made from a biodegradable polymer having a first degradation rate and an outer section made from a blend of a first biodegradable polymer component and a second biodegradable polymer component covering the exterior surface of the inner core and having a second degradation rate; where the second degradation rate is lower than the first degradation rate.

Abstract: A prosthetic socket is fitted at a distance from its distal end with an annular chamber. This annular chamber is closed by a contour-conforming sealing wall facing the inner side of the prosthetic socket, said wall being designed to hermetically rest against the outer side of a residual limb. The space between the contour-conforming wall and the hard prosthetic socket is vented to atmosphere, whereby self-enhancing compression by the sealing wall against a residual limb arises when a partial vacuum arises in the distal prosthetic socket between the wall and the distal end. A liner having a sealing wall also is disclosed.