Abstract: Systems and methods employ functional instruments to close incisions and wounds using a suture knot in combination with a biocompatible material composition. The systems and methods are well suited for use, for example, at a vascular puncture site following a vascular access procedure.

Abstract: An apparatus for receiving and positioning a medical instrument relative to the body of a patient when the instrument is positioned partially within the body or completely outside the body. The apparatus comprises a housing and a motor assembly positioned within the housing. The motor assembly includes a motor and a first medical instrument engaging member operatively connected to the motor and moveable relative to the housing in response to the operation of the motor. A second medical instrument engaging member cooperates with the first medical instrument engaging member to drive the medical instrument within the housing when the medical instrument is positioned within the housing between the first and second medical instrument engaging members. The apparatus can form a portion of a trocar, a structure secured to a trocar or a structure that is free of a connection to a trocar or other medical instrument support.

Abstract: A vascular occlusion device deployment system for deploying an occlusion device at a preselected site within the vasculature of a patient. The deployment system includes a pusher which has a constrictor located at the distal end portion of the pusher. The constrictor has a channel which receives a portion of the occlusion device. The constrictor has a proximal end portion and a distal end portion wherein the proximal end portion can be moved relative to the distal end portion to reduce the size of the channel. When the channel size is reduced, the constrictor grasps the portion of the occlusion device located within the channel. When it is desired to deploy the coil, the constrictor is moved in the opposite direction to increase the size of the channel and release the coil's grasp of the occlusion device.

Abstract: A coupling system is disposed at the distal end of an interventional delivery system for coupling to an implant. The coupling device has a first and second prong connected at one end. The other end of the prongs open or close to release or trap an object, e.g., a bead tethered from an implant. A slot at the distal end of the coupling device allows extra degrees of flexibility for the coupling device.

Abstract: The present disclosure is directed to a medical device or article that reduces the ability of the Keith needle to unintentionally fall out of the barrel, improves the ability of the Keith needle to track on axis, or both. In one aspect, the disclosure is directed toward a medical device suitable for use in implant surgery. The medical device includes a Furlow insertion tool with a barrel having a bore. The Furlow tool further includes an obturator adapted for slidable insertion into the bore. The medical device further includes a Keith needle adapted for slidable insertion into the bore. The Keith needle is adapted to yieldably fit against at least one of the barrel and the obturator when the Keith needle is disposed within the bore. In another aspect, the present disclosure is directed toward a Keith needle adapted for use with a Furlow insertion tool. The Furlow insertion tool including a barrel and an obturator.

Abstract: Systems, including apparatus and methods, for repairing injured connective tissue. These systems may include, among others, a surgical stapler and staples for repairing partially or completely severed tendons and/or ligaments.

Abstract: A medical device can be used to entrain biological or foreign material during a medical procedure for the fragmentation of the material. The device also can be used to remove the material safely from the body. The device has a core element with a first portion extending substantially longitudinally and a second portion wound to form at least a helical coil in the shape of cone. A flat wire can substantially wrap the first and second portions of the core element, or a wire can substantially wrap the first portion and a sheath can substantially cover the second portion.

Abstract: A strut assembly to be used in conjunction with an embolic filtering device has varying strut thicknesses, with the thickness selected based at least in part on the flexing characteristics of the particular portion of the strut assembly. The strut assembly is formed with patterns having flexing portions and stable portions, with the flexing portions contributing to the flexibility of the strut assembly during delivery and recovery in the patient's vasculature. The stable portions remain relatively unflexed and stiff when being delivered or recovered from the patient's vasculature. The stable portions provide strength and increased radiopacity to the strut assembly which is needed when the strut assembly is deployed in the body vessel. The flexing portions act much like a mechanical hinges in providing the needed flexibility to resiliently bend when being delivered through tortuous anatomy of the patient.

Abstract: A cycling suturing and knot-tying device is characterized by an arcuate fixed, grooved or recessed way provided in a correspondingly-shaped support frame for accommodating a curved needle fitted with thread, and frictional needle-engaging devices provided in the way for selectively engaging the needle and driving the needle in one or both rotational directions to suture a wound with the thread. Selective articulation of the frame and the way and driving of the needle in the way by positioning the frictional needle-engaging devices with respect to the needle are typically effected by manipulation of a pistol-grip operating apparatus having a transmission tube that mounts the frame and the way in articulating relationship and rotates and articulates with respect to the pistol grip and carries various operating elements that interface with the frictional needle-engaging devices in the way.

Abstract: A high-speed pneumatic cutting system having a cutter and an actuator. The cutter is a guillotine-type, pneumatic cutter that receives a train of pressure pulses from the actuator. The actuator is designed to capture pressure pulses it receives from a pneumatic energy source in a surgical machine, such as a vitrectomy machine, or to generate its own pneumatic energy. The actuator has an accumulator coupled to the outlet of the pneumatic energy and a pressure transducer that senses the pressure level inside the accumulator. A control and display unit with a plurality of input mechanisms receives inputs from a user who selects a desired cutting rate or frequency for the cutter. The control and display unit produces an output signal based on the inputs received. The outputs from the control and display unit and the pressure transducer are sent to a waveform shaping circuit. The waveform shaping circuit produces a command signal based on the inputs that it receives.

Abstract: The present invention discloses a seamless pad-type filter which is characterized in that it comprises two co-extensive sides, a top side and a bottom side. The top and bottom sides are made of fluid filtration material. The two sides create an inner chamber therebetween and are surrounded and joined together by a seamless outer perimeter. The seamless outer perimeter providing a seamless folded continuity between the two sides of the pad-type filter in the form of a plurality of fold lines which, as connecting segments beginning and ending at the same point, define the seamless outer perimeter. The top side further comprising a plurality of positive and negative secondary creases formed around a plurality of positive and negative crease lines. The crease lines are inclined to the fold lines and form pleats.

Abstract: A stapling unit for use with an endoscopic stapling system adapted to be advanced along an endoscope to a predetermined location within a body lumen to staple the portion of tissue, as part of an occlusal or full thickness resectioning procedure. The stapling unit comprises a first casing having a distal end, a proximal end and a stapling device mounted thereto adjacent to a first window extending through a periphery of the first casing. The invention includes methods for the stapling, severing and removal of tissue by using the device.

Abstract: An apparatus for inhibiting blood loss from a puncture site. The apparatus may include means for locating a puncture site in a blood vessel wall. This apparatus is comprised of a tube and an elongated member that is positioned around the tube. The elongated member includes a proximal end and a distal end. Around the tube is also a dissolvable distal capsule, the distal capsule including a proximal end and a distal end, wherein the proximal end of the distal capsule attaches to the distal end of the elongated member. Inside the distal capsule is hemostatic material such as a sponge.

Abstract: Improvements to external stents to render incompetent venous valves competent are disclosed. The device is an inelastic bio-compatible cuff (1) that encircles the venous valve cusps (15) decreasing the internal diameter of the vein wall (11) to allow apposition of the cusps (15) and create competence. The device may be calibrated to known diameters to create competence for different phenotypes. The different diameters are indicated by holes (2, 3, 4) in the body (1). The buckle attachment (6) allows the body of the device to become conical or inverted to become pyramidal as appropriate. The wide buckle (5) allows the device to become elliptical at smaller diameters. The angle of the notches (10) in the device is approximately 15°, which allows better overriding at the sapheno-femoral junction resulting in better competence of the valve.

Abstract: A device and method for achieving hemostasis and leakage control in vascular structures and other body ducts or vessels in an emergency room or trauma situation. The device has at least one shunt that contains an obturator on an end of the shunt. The shunt is inserted into a damaged vessel or lumen for sealing the leak or hemorrhage. Two shunts that both contain obturators on one of their ends can be inserted into two different vessels or lumens when the vessel or lumen has been severed. The obturators allow for the improved ease of insertion into the vessel or lumen. The two shunts are then releasably attached to restore fluid communication through the vessel or lumen. The shunt is placed temporarily within the patient and then removed when definitive repair can be achieved by a qualified physician.

Abstract: An piercing member is axially fixed to and positioned within a cutter, both of which are components of a stand-alone tool for creating an opening in the wall of a tubular tissue structure. The stand-alone tool includes an impulse source connected to the piercing member and to the cutter. An actuator is operationally connected to the impulse source, where the actuator causes the impulse source to release energy to and provide an impulse to the piercing member and the cutter. The tool may be configured to make multiple openings in the tissue of the same patient. Where the tool is configured to make multiple openings in the tissue of the same patient, the tool allows the piercing member and cutter to be moved back to an initial pre-deployment position after each use.

Abstract: These and other objects of the present invention are achieved in a body fluid sampling system for use on a tissue site that includes an electrically powered drive force generator. A penetrating member is operatively coupled to the force generator. The force generator moves the member along a path out of a housing having a penetrating member exit, into the tissue site, stops in the tissue site, and withdraws out of the tissue site. A cartridge houses the penetrating member. The cartridge has first and second seals coupled to the penetrating member to maintain a sterile environment around a portion of the penetration member prior to penetrating member actuation. A user interface is configured to relay at least one of, penetrating member performance or a penetrating member setting.

Abstract: When a guide wire is inserted into a guide wire insertion hole formed in a tip member made of a resin tube, firstly, it is inserted into the guide wire insertion hole substantially from the center of the front surface of the resin tube. Then, the guide wire is guided to the outside of the resin tube through an opening formed in the outer periphery of the tube, and guided along the outer periphery of a basket unit.

Abstract: Surgical methods and related medical devices for treating glaucoma are disclosed. The method comprises trabecular bypass surgery, which involves bypassing diseased trabecular meshwork with the use of a stent implant. The stent implant is inserted into an opening created in the trabecular meshwork by a piercing member that is slidably advanceable through the lumen of the stent implant for supporting the implant insertion. The stent implant is positioned through the trabecular meshwork so that an inlet end of the stent implant is exposed to the anterior chamber of the eye and an outlet end is positioned into fluid collection channels at about an exterior surface of the trabecular meshwork or up to the level of aqueous veins.

Abstract: The disclosed method of monitoring the cuff pressure of an LMA provides an estimation of a patient's anesthetic state. Cuff pressure tends to rise and fall during IPPV and spontaneous breathing. One of the disclosed methods activates an alarm if an instantaneous value of the cuff pressure exceeds selected levels. This method may also automatically adjust the selected levels. One of the disclosed methods activates an alarm if activity of the cuff pressure as observed over a period of time exceeds a selected level.