Abstract: A brachytherapy device for treating tissue within a cavity of a body. The device may include a first set of tubes configured to be inserted into the cavity through an opening at the surface of the body. Each of the tubes may have an external end and an interior channel beginning at the external end that is configured to receive radioactive material. The external ends of the tubes may be bundled together. The tubes may be of a length that causes the external ends to be near the opening in the surface of the body while the tubes are in the cavity. A seal may be configured to prevent fluid that originates from the cavity from entering into the external ends of the tubes while they are near the opening in the surface of the body. The seal may include a gasket that is pressed against the external ends of the tubes. The gasket may have openings that align with channels within the external ends of the tubes.

Abstract: An apparatus and method are disclosed for treating overweight and obese patients by applying a restrictive Artificial Gastric Valve (AGV) on part of the stomach. The apparatus includes a mechanism to control the opening of the AGV automatically on demand, dynamically and progressively. The controlled opening of the AGV inside the stomach controls and regulates the flow of food.

Abstract: An apparatus including a flexible length of cord and three tissue connectors positioned at the opposite ends of the cord and at an intermediate position of the cord is designed to be laparoscopically inserted through the abdominal wall and into the abdominal cavity, and used to move a first internal organ to a position away from a second internal organ where the apparatus holds the first internal organ in the position without further manual input, thereby providing surgical access to the second internal organ.

Abstract: The invention relates to an implant for treating a cavity that is created as a result of a resection, the implant being modular and the modules being interconnectable.

Abstract: Device for implementing endovascular brachytherapy, whereby in the region of the catheter tip, a beta or gamma radiator used to prevent restenosis after the removal of plaque from vessel walls emits radioactive radiation in order to suppress the structural vessel alteration, with simultaneous OCT-monitoring, whereby a brachytherapy is combined with an OCT catheter in an integrated unit.

Abstract: In an embodiment, a brachytherapy device includes a cartridge adapted for use with a brachytherapy applicator. A plurality of therapeutic members are stacked parallel to one another within the cartridge. Each therapeutic member includes a radioactive seed that is at least partially encapsulated by a polymeric material. Additionally, each therapeutic member can include at least one protrusion on an outer surface of the encapsulating polymeric material to reduce a tendency for the therapeutic member to migrate and rotate within a patient's body after the therapeutic member is implanted.

Abstract: A system and method for locating an internal device separated by a boundary from and in wireless communication with an external device. External device includes an active emitter mechanism wherein a carrier signal is modulated by a location interrogation signal thereby generating an external RF power signal during transmission to the internal device. A secondary antenna of the internal device receives the external RF power signal and induces an RF power signal therein that is converted to a DC induced voltage signal. An indication signal proportional to the intensity of the DC induced voltage signal induced in the secondary antenna is produced by the external device. The process is repeated each time the user moves the external device to a new location proximate the patient's body until a maximum DC induced voltage signal measurement is ascertained representative of a specific area in which the internal device is located.

Abstract: A therapeutic member for use in brachytherapy deliverable to an implant site by way of a needle comprises a single radioactive source encapsulated by a bio-absorbable material having an outer surface including one or more ribs encircling the single radioactive source, a leading edge endcap rib and a trailing edge endcap rib. The one or more ribs reduces a tendency of the member to migrate and rotate within a patient's body after implantation. The encapsulating material further includes a first rail formed from the bio-absorbable material extending at least from opposite sides of the outer surface of the encapsulating material along the longitudinal axis of the therapeutic member, and a second rail formed from the bio-absorbable material extending at least from opposite sides of the outer surface of the encapsulating material along the longitudinal axis of the therapeutic member, the second rail arranged in a plane substantially perpendicular to a plane in which the first rail is arranged.

Abstract: Various exemplary methods are disclosed for implanting a restriction device for forming a restriction in a patient. The methods can be used with a variety of restriction devices, but in an exemplary embodiment the methods are used for implanting a gastric restriction device.

Abstract: A surgical implant for supporting pelvic anatomy includes a first fixing zone, a second fixing zone, and a supporting zone. The first fixing zone has a retaining portion that is absorbable and formed of a fiber entanglement and a mesh for anchoring the first fixing zone in soft tissues in a space defined by a pelvis. The second fixing zone has a retaining portion that is absorbable and formed of a fiber entanglement and a mesh for anchoring the second fixing zone in soft tissues in a space defined by a pelvis. The supporting zone is formed of a mesh and is interposed between the first and second fixing zones.

Abstract: A method for supporting a urethra of a patient includes making an incision on an upper wall of a vagina of the patient and inserting a first end of a surgical implant through the incision and on a first side of a urethra of the patient. The first end of the surgical implant has a first fixing zone with a retaining portion that is formed of a fiber entanglement and a mesh.

Abstract: Combined brachytherapy and ablation devices and methods. A combined brachytherapy and cryotherapy method, includes: inserting an ablation device into tissue of a subject; ablating tissue within an ablation zone of the device; detaching and removing a first part of the device while leaving a second part of the device in the tissue, the first part contacting the ablation zone; and inserting a brachytherapy rod into the second part of the device when the second part is detached from the first part, the brachytherapy rod connected to base at one end and retaining at least one radioactive seed at an opposing end, the brachytherapy rod configured and dimensioned so that when it is inserted into the device up to the base, the at least one radioactive seed is in the ablation zone.

Abstract: A blood vessel preservation device is disclosed comprised of a vessel cannister, cannister cap, vessel alignment insert, pulsatile pump and both inlet and outlet tubing. The vessel canister is advantageously configured as a hollow tube-like structure with a central bore having one open terminus—the proximal terminus—and a closed distal terminus—similar to a large test tube—. Integrated embodiments of the device are disclosed wherein blood is provided from natural circulation and returns thereto. Non-integrated embodiments are also disclosed wherein sufficient blood is provided to the device and thereafter the device functions separate and apart from a patient's circulatory system.

Abstract: Methods and devices for treating female urinary incontinence by injecting bulking material into the female urethral wall. Some devices include a handle, an elongate member attached to the handle, and a vacuum generating syringe removably secured to the handle. The elongate member can include a distal portion projecting distally from the handle, the distal portion having a wide proximal region, a narrowing shoulder, and a narrow distal region. The elongate member can include one or more vacuum ports on either side of the shoulder region. The shoulder can include a distally facing needle aperture allowing passage of a needle for injecting bulking agent. A rotatable connection between the elongate member and the handle facilitates rotatable positioning of the elongate member to permit injection of bulking material at different locations around the urethral wall.

Abstract: A system for supporting an anatomical structure of the pelvis includes a surgical implant for providing support to the anatomical structure of the pelvis. The surgical implant includes a first tissue anchor including a plurality of projections adapted for tissue fixation, a second tissue anchor including a plurality of projections adapted for tissue fixation, and a sub-urethral support having first and second ends, the first and second tissue anchors extending from the first and second ends of the sub-urethral support. The system also includes an introducer for delivering the first tissue anchor to a desired anchoring site of the pelvis.

Abstract: A vessel preparation and preservation kit supports a blood vessel during processing for use in bypass graft surgery. The device comprises a clamshell base having first and second trays latchable in a closed condition and pivotable to an open condition. The first tray has a series of open slots on an interior surface, wherein each slot extends substantially transverse to the longitudinal axis of the clamshell base. A first fixture has a first plate positionable in any selected one of the slots, a first fitting for holding a first end of the blood vessel, and a fluid supply needle for inserting into the first end of the blood vessel. A second fixture has a second plate positionable in any selected one of the slots a predetermined distance from the first fixture and having a second fitting for holding a second end of the blood vessel. A liquid-retaining foam is mounted in the second tray to immerse the prepared blood vessel in liquid to preserve it by putting the trays in the closed condition.

Abstract: In an embodiment a therapeutic member includes a solitary radioactive seed. The seed includes a metallic housing with radioactive material contained within the metallic housing. The metallic housing has a first longitudinal end and a second longitudinal end and a longitudinal length between the first and second longitudinal ends. A polymeric material is molded to completely and monolithically encapsulate the metallic housing of the solitary radioactive seed. The implantable therapeutic member is adapted to be implanted into patient tissue using a hollow needle. A portion of the molded polymeric material extends from one of the first and second longitudinal ends of the metallic housing to reduce a tendency of the seed to migrate and rotate within a patient's body after implantation of the member.

Abstract: A coronary artery bypass grafting device includes a plurality of attachment members each having: a flexible tube (102); a suction cup portion (101) provided in a tip end side of the flexible tube (102); a three-way cock (103) provided in the flexible tube (102); and a holding member (104) that holds the flexible tube (102). At least one of the attachment members further includes a duckbill valve (111) provided in the flexible tube (102).

Abstract: A surgical device for localized delivery of beta radiation in surgical procedures, particularly ophthalmic procedures. Preferred surgical devices include a cannula with a beta radiotherapy emitting material at the distal end of the cannula. The surgical device is particularly suitable for use in the treatment of treat Age Related Macular Degeneration (AMD).

Abstract: An apparatus for providing a restriction and sensing an associated operational parameter, comprises a restriction device and a sensing device. The restriction device is configured to be secured around a portion of an anatomical structure. The restriction device is operable to form a restriction within the anatomical structure. The sensing device is configured to sense a parameter associated with operation of the restriction device. At least a portion of the sensing device is configured to be positioned adjacent to tissue of the anatomical structure. The restriction device may comprise a gastric band, among other things. The sensing device may comprise a pressure sensor, among other things.