Abstract: An intravascular occlusion balloon catheter having a removable hub, a profile sized to approximate a guidewire, and a means for venting air from the balloon. The removable hub and the small profile allow the occlusion balloon catheter to be used as a guidewire. The venting means allows air to be easily and reliably removed from the balloon prior to use.

Abstract: Described are devices useful to deliver fluid to tissue of the bladder, bladder neck, prostate, urethra, ureter, kidney, and related methods, the devices including one or a combination of features such as a steerable shaft, an optical mechanism, multiple fluid delivery orifices that may be moveable or extendable laterally, longitudinally, or distally; the methods allowing for delivery of one or multiple types of fluid to tissue such as the bladder (including the bladder neck), urethra, prostate, kidney, ureter, etc.

Abstract: Improved anastomosis devices having structural upgrades to increase ease of use while simultaneously increasing patient safety. The anastomosis device can include a distal treatment end and a proximal connection end. The anastomosis device has a catheter portion with a plurality of inflation lumens and a funnel portion. The funnel portion includes access ports in fluid connection to a catheter receiving aperture for attaching to the catheter portion. Also, the access ports including a drainage port, a control port and a plurality of inflation ports.

Abstract: A needleless fluid delivery system for delivering therapeutic fluids to treatment sites within a patient. The fluid delivery system can include an automated injector source and a needleless access device. The access device can include a delivery scope and a treatment specific applicator. The automated injector source, delivery scope and applicator can be operably coupled with quick-connect style fittings so as to allow for quick replacement and maintenance of used or damaged components. The automated injector source can include a hands-free input mechanism allowing a medical professional to use both hands in manipulating the delivery scope and needleless applicator at the same time an injection is desired. The delivery scope and needleless applicator can comprise flexible or rigid lengths of tubing based on the accessibility of the treatment site. The needleless delivery system can include an imaging system for precisely position the applicator with respect to the treatment location.

Abstract: An anastomosis device providing increased functionality, reliability and safety through the use of designs addressing potential puncture of an inflation balloon being used to hold and approximate tissue. The anastomosis device can include bladder retention structures configured to engage and retain tissue without pointed or sharpened surfaces that can rupture the inflation balloon. The anastomosis device can include a reinforced or otherwise protected inflation balloon to resist puncturing by a bladder retention structure. The anastomosis device can include a catheter wall profile selected to physically prevent bladder retention structures from being forcibly bent back so as to avoid potential contact with and puncture of the inflation balloon. The anastomosis device can include a catheter funnel with an internal spring for preventing kinking of the catheter lumen while providing for flexibility and stretch of the funnel to absorb pulling or shock force which can rupture the inflation balloon.

Abstract: An improved x-ray brachytherapy system and related methods for delivering low dose radiation to a treatment location while minimizing damage to surrounding healthy tissue. Generally, the x-ray brachytherapy system can include a device controller, a device positioner, system imagery, and an x-ray brachytherapy probe having two or more delivery needles. The two or more delivery needles are operably coupled to at least one probe housing such that a tip spacing between the delivery needles is minimized when positioned at the treatment location. By reducing tip spacing at the treatment location, smaller radiation doses can be delivered so as to limit radiation exposure to surrounding healthy tissue.

Abstract: A surgical tool which comprises an elongated body having a proximal end and a distal end, first and second sets of tissue approximating structures having deployed and retracted positions relative to the elongated body, an actuating mechanism extending from the proximal end of the elongated body for independently deploying and retracting each of the first and second sets of tissue approximating structures, a drainage lumen extending from a drainage aperture at the distal end of the elongated body to the proximal end, a main balloon adjacent to the distal end of the elongated body, and a strap connector extending from the elongated body that is connectable with a stabilization strap.

Abstract: A surgical tool including an elongated body having a proximal end and a distal end, first and second sets of tissue approximating structures having deployed and retracted positions relative to the elongated body, an actuating mechanism at the proximal end of the elongated body for independently deploying and retracting each of the first and second sets of tissue approximating structures, and a drainage lumen extending from a drainage aperture at the distal end of the elongated body to the proximal end. The tool further includes a main balloon adjacent to the distal end of the elongated body, wherein the first set of tissue approximating structures has a different configuration than the second set of tissue approximating structures.

Abstract: The anastomosis devices of the invention advantageously provide reinforcement structures or components that increase the strength and/or flexibility of the device. These features can be especially beneficial to protect the integrity of the installation of the device within a patient to facilitate the healing process. These features may provide resistance to tearing or ripping of the catheter body or sheath by the tissue approximating structures and/or may provide strength in other areas of the catheter body. The anastomosis devices of the invention may further include method and devices for placing markers on the anastomosis device to facilitate accurate placement of the device within the patient.

Abstract: Described are surgical implants, tools, systems, and related methods, useful for implantation of surgical implants, such as those used to treat pelvic conditions including incontinence.

Abstract: Described are surgical implants that include a central support portion adapted to be positioned to support pelvic tissue, between mesh end portions adapted to be passed through body tissue, wherein edges of the end portions exhibit extensions that are resistant to deformation.

Abstract: Connectors for interconnecting rods, fixed to vertebrae and other bones of a subject include a body portion and two recesses or pockets for receiving the rods. These connectors are generally able to be secured to the rods by a tightening a fastener or retaining member from above the spine, which can facilitate the procedure for the surgeon. The connectors can include rotatable or stationary pockets, mating members that pivot and/or translate within the coronal plane of the subject to adjust to the positions of the rods, and extension shafts that pivot to adjust for rod angle.

Abstract: An orthopedic fixation connector and system is provided. The orthopedic fixation system includes bone anchors and linking elements that are coupled together to form a stabilization construct. The linking elements are fixed relative to the bone anchors by clamping arrangements. The clamping arrangements include first linear interlock components coupled to the anchors and second linear interlock components that linearly interlock with the first interlock components to clamp the linking elements at desired positions relative to the anchors.

Abstract: An intravascular occlusion balloon catheter having a removable hub, a profile sized to approximate a guidewire, and a means for venting air from the balloon. The removable hub and the small profile allow the occlusion balloon catheter to be used as a guidewire. The venting means allows air to be easily and reliably removed from the balloon prior to use.

Abstract: An intravascular occlusion balloon catheter having a removable hub, a profile sized to approximate a guidewire, and a means for venting air from the balloon. The removable hub and the small profile allow the occlusion balloon catheter to be used as a guidewire. The venting means allows air to be easily and reliably removed from the balloon prior to use.

Abstract: A dilation catheter having a first shaft section, a second shaft section attached to the first shaft section, and an inflatable balloon attached to the second shaft section. A fluid pathway is defined through the catheter for inflation of the balloon. A guide wire lumen is provided in the second shaft section that can extend between the distal end of the balloon and a point distal of the first shaft section. A stiffening member is provided within the second shaft section of the dilation catheter to provide additional stiffness to the second shaft section. In a preferred embodiment, the stiffening member is attached at the distal end of the first shaft section to occlude the hollow passage of the first shaft section. In this embodiment, the first shaft section farther includes a fluid port that is proximal of the stiffening member and that extends between the hollow passage of the first shaft section and the exterior of the first shaft section.

Abstract: A body implantable stent is formed of a plurality of strands arranged in two sets of coaxial helices, wound in opposite directions to form multiple crossings. At selected crossings, the adjacent strands are welded to one another, while at the remaining crossings the strands are free for limited movement relative to one another. The welds are formed in patterns that preferably enhance radial strength and rigidity, while having a minimal impact on axial bending flexibility. Preferred weld patterns in this regard include rings or circumferential rows, and helices, particularly with a steeper pitch than that of the strands. Stent fabrication preferably involves resistance welding at the crossings, and use of a tool to reuniformly compress the stent around and against the distal end region of a balloon catheter used later to deliver the stent to a treatment site.

Abstract: A dilation catheter having a first shaft section, a second shaft section attached to the first shaft section, and an inflatable balloon attached to the second shaft section. A fluid pathway is defined through the catheter for inflation of the balloon. A guide wire lumen is provided in the second shaft section that can extend between the distal end of the balloon and a point distal of the first shaft section. A stiffening member is provided within the second shaft section of the dilation catheter to provide additional stiffness to the second shaft section. In a preferred embodiment, the stiffening member is attached at the distal end of the first shaft section to occlude the hollow passage of the first shaft section. In this embodiment, the first shaft section further includes a fluid port that is proximal of the stiffening member and that extends between the hollow passage of the first shaft section and the exterior of the first shaft section.

Abstract: A body implantable stent is formed of a plurality of strands arranged in two sets of coaxial helices, wound in opposite directions to form multiple crossings. At selected crossings, the adjacent strands are welded to one another, while at the remaining crossings the strands are free for limited movement relative to one another. The welds are formed in patterns that preferably enhance radial strength and rigidity, while having a minimal impact on axial bending flexibility. Preferred weld patterns in this regard include rings or circumferential rows, and helices, particularly with a steeper pitch than that of the strands. Stent fabrication preferably involves resistance welding at the crossings, and use of a tool to reuniformly compress the stent around and against the distal end region of a balloon catheter used later to deliver the stent to a treatment site.

Abstract: To improve the re-wrappability of the expander members used on balloon catheters subsequent to an initial inflation thereof, the balloon member is subjected to an annealing process in which the balloon member, in its wrapped configuration, is placed within a plastic sheath and it, together with the sheath, is then placed between the jaws of a clamping fixture where the jaws may be heated to a predetermined temperature. When the jaws are made to close on the sheath and the wrapped balloon contained within it, the wrapped balloon is subjected to a radial compressive pressure and a temperature approximately equal to or above the glass transition temperature for the balloon material utilized and then maintained at that temperature for a predetermined time interval. The annealing is found to introduce a memory component into the plastic of the balloon that causes it to assume a lower profile upon deflation than otherwise obtained.