Abstract: Apparatus, including a current source which has a transformer having a primary winding coupled to receive input power. The transformer has a secondary winding having a first plurality of secondary taps configured to supply electrical power at an ablation frequency to an electrode in contact with body tissue. The tissue has an impedance, and is ablated by the electrical power. The current source has a second plurality of capacitors. The apparatus also includes a controller which is configured to select one of the secondary taps and at least one of the capacitors in response to the impedance and the ablation frequency, and to connect the selected secondary tap to the selected at least one of the capacitors.

Abstract: Apparatus, including an energy generator, configured to supply first ablation power modulated at a first frequency and second ablation power modulated at a second frequency different from the first frequency. The apparatus also includes a probe, having at least one electrode coupled to receive the first and second ablation powers simultaneously and to dissipate the first and second ablation powers in body tissue in contact with the at least one electrode.

Abstract: An atrial ablation catheter with an electrode array particularly adapted to locate and ablate foci of arrhythmia which are required for sustained atrial fibrillation is provided. The array is easily deployed and retracted from the catheter, and presents a proximally oriented electrode array that can be pulled against the septal wall of the left atrium to engage the septal wall.

Abstract: Systems, delivery devices, and methods to treat to ablate, damage, or otherwise affect tissue. The treatment systems are capable of delivering a coolable ablation assembly that ablates targeted tissue without damaging non-targeted tissue. The coolable ablation assembly damages nerve tissue to temporarily or permanently decrease nervous system input.

Abstract: A device may include a sheath including a lumen, a distal end, and a proximal end. The device may further include an end-effector unit and an elongate member connected to the end-effector unit. The end-effector unit and the sheath may be movable relative to each other to achieve a first state of the end-effector unit and a second state of the end-effector unit. Moreover, the medical device may include a handle having a first handle portion connected to the proximal end of the sheath, a second handle portion connected to the proximal end of the elongate member, and a compliant member longitudinally aligned with the sheath between the first handle portion and the second handle portion. The first and second handle portions may be configured such that relative movement of the first and second handle portions causes the end-effector to move between the first and second states.

Abstract: A medical instrument is provided for a ablating tissue. The medical instrument has an inner bipolar electrode and an outer bipolar electrode. The inner and outer electrodes are separated by an insulation layer. The inner and outer electrodes form a loop that may be rotated around a tumor to ablate the tumor tissue.

Abstract: A surgical instrument configured to deliver electrical energy to tissue of a patient includes a handle, a first conductor, and a second conductor. The surgical instrument further includes a first electrode with a first distal portion, a second electrode with a second distal portion, and a third electrode with a third distal portion, wherein each distal portion is configured to contact the tissue. The second distal portion surrounds the first distal portion and the third distal portion surrounds the second distal portion. A first gap is defined between the first distal portion and the second distal portion. A second gap is defined between the second distal portion and the third distal portion. The first electrode includes a sharp end configured to penetrate the tissue and the second distal portion includes a plurality of projections extending toward third distal portion.

Abstract: In various embodiments, a surgical instrument is provided that may comprise an end effector for performing a surgical procedure on tissue, for example. The end effector may comprise at least one energy delivery surface and heat dissipation means for dissipating heat from at least a portion of the end effector. For example, in at least one embodiment, the end effector may comprise a first jaw, a second jaw, and a cutting member. The cutting member may comprise a cutting surface and a body, which may define a cavity and at least one opening communicating with the cavity. A fluid may be moved through the cavity to and/or from the opening(s). Additionally, in at least one embodiment, a surgical instrument's end effector may comprise a first jaw, a second jaw, a cutting member, and at least one heat pipe. Various other heat dissipation means are also disclosed.

Abstract: A bipolar electrosurgical instrument is provided. The bipolar electrosurgical instrument includes first and second shafts each having a jaw member extending from a distal end thereof and a handle disposed at a proximal end thereof for effecting movement of the jaw members relative to one another. A first conductive lead is adapted to connect to a first electrical potential and a second conductive lead is adapted to connect to a second electrical potential. One of the first and second conductive leads extends through the pivot to connect to a respective jaw member.

Abstract: The invention relates to a device for providing skeletal support. A bone support device comprising an upright rod having a proximal and a distal end; at least one support member located near the proximal end for securing the rod to the bone; at least one distal anchoring element; and a vent member is provided.

Abstract: The present invention relates to a percutaneous implant abutment for bone anchored implant devices adapted to be anchored in the craniofacial region of a person, such as bone anchored hearing aids. The abutment comprises a skin penetration body having a skin contacting surface. The skin contacting surface has been modified.

Abstract: A surgical instrument system functional in multiple orthopedic applications, including but not limited to shoulder, knee, hip, wrist, ankle, spinal, or other joint procedures. The system comprises a cutting head which includes jaw members which may be urged between open and closed positions to providing a biting or chewing action for removal of targeted tissues. The instrument system is configured to be driven by an attached hub that translates a rotational movement into a reciprocating motion to open and close the jaw members. Suction for removal of bone fragments or other tissues is provided through a suction opening.

Abstract: Treatment of spinal irregularities, including, in one or more embodiments, derotation apparatus and systems that can be used to reduce the rotation of vertebral bodies. Derotation apparatus that may comprise a tube assembly comprising an inner sleeve and an outer sleeve disposed over the inner sleeve. The inner sleeve may have a distal end for attachment to an implant. The tube assembly may further comprise a handle assembly. The tube assembly may further comprise a ball joint assembly disposed between the tube assembly and the handle assembly. The ball joint assembly may comprise a ball joint configured for attachment to a coupling rod. The ball joint assembly further may comprise a reducing extension below the ball joint, the reducing extension being sized to fit in a central bore of the inner sleeve. Orthopedic fixation devices comprising a ball joint are also disclosed.

Abstract: Rod insertion tools, rods and methods for placing rods in patients are described. An exemplary spinal rod insertion tool comprises a handle, a main body connected to the handle, a rod engaging member disposed within an inner passageway defined by the main body and adapted to move from an extended position to a chambered position in which the rod engaging member distal end is disposed within the inner passageway, and an adjustment mechanism operably connected to the rod engaging member and adapted to cause movement of the rod engaging member from the extended position to the chambered position.

Abstract: A low profile bone screw system includes a retainable washer and a low profile bone screw having a smooth conical head for insertion into the washer. The washer has an axial bore with a conical portion for fully seating the screw head and a smooth outer surface shaped like the head of a conventional compression bone screw head. Washer dispensing units are also provided for assembling screw and washer assembled units.

Abstract: Patient specific surgical instruments, and in particular cutting guides, and methods of use and manufacture are described. The surgical instrument can be used in an orthopaedic arthroplasty procedure to be carried out on a joint of a patient and can allowing soft tissue balancing for the joint. The instrument comprises a body having an attachment area configured using data specific to a bone of the joint of the patient so as to attach to the bone in a unique position. The instrument includes at least a first cutting guide and an adjustment mechanism operable to change the position of the cutting guide relative to the bone.

Abstract: An instrument for setting ligament tension between a distal femur and a proximal tibia has a rod mounted on a femur. The rod has an extension extending along a first axis. A first drive element is mounted on the distal femur and is rotatable about a second axis. A body is rotatably mounted on the rod extension for rotation about the first axis. The body has a second drive element engaging the first drive element and a third drive element extending about a third axis offset from the first and second axes. A ligament tensioning element is mounted on the body and has a foot for engaging a posterior condyle of a femur and has a fourth drive element. A fifth drive element engages both the third and fourth drive elements for moving the ligament balancer with respect to the body along the third axis.

Abstract: An instrument for performing a medical procedure includes a drive shafts a holding clutch, a drive clutch, and an actuator. The holding clutch only allows advancement of the drive shaft, while the drive clutch transfers an advancement force from the actuator to the drive shaft. The dual clutch system allows a lever to be used as the actuator so that a user can generate large actuation forces manually (and optionally remotely) without significant physical effort. This capability can beneficially improve the usability and effectiveness of percutaneous surgical systems, such as those for vertebroplasty or kyphoplasty.

Abstract: The present invention relates in certain embodiments to medical devices for treating vertebral compression fractures. More particularly, embodiments of the invention relate to instruments and methods for controllably restoring vertebral body height by controlling the flow of bone cement into the interior of a vertebra and the application of forces causes by the cement flow. An exemplary system utilizes Rf energy in combination a conductive bone cement for selectively polymerizing the inflow plume to increase the viscosity of the cement. In one aspect of the invention, the system utilizes a controller to control bone cement flow parameters to either allow or disallow cement interdigitation into cancellous bone. A method of the invention includes pulsing the flows of bone cement wherein high acceleration of the flow pulses can apply expansion forces across the surface of the cement plume to reduce a vertebral fracture.

Abstract: An apparatus and method for positioning a guide tube fixation device at a spinal structure of a patient are provided. The method includes attaching an attachment element to the spinal structure, attaching a guide tube to the attachment element, wherein said guide tube is calibrated prior to attachment, and navigating a part of the guide tube to a predetermined location relative to a target region of the patient. The apparatus includes an attachment device for attaching to the spinal structure, a joint attached to the attachment device, and a guide tube holding device attached to the joint and operable to hold and/or guide a guide tube, said guide tube configured to guide a cannula, needle and/or fluid to a desired site or location.

Abstract: A device serves for guiding a drilling tool for forming a second bore in a bone, which second bore intersects an already existing first bore. A frame, having a first end and a second end has a rod-shaped body arranged at its first end. Said rod-shaped body is designed to be inserted into said already existing first bore. A guide sleeve is arranged at said second end of said frame and has a longitudinal axis intersecting said rod-shaped body in an area of its distal end. A fixing device is provided at said guide sleeve, said fixing device protrudes distally from said guide sleeve, said protruding fixing device can be placed on a body of a patient to be treated in an area where said second bore is to be formed.

Abstract: A controlled force surgical implant impaction instrument is provided which includes a striking assembly, a retaining pin, and an actuator component. The striking assembly is configured to impact a surgical implant. The retaining pin is moveable between a first position and a second position. In the first position, the retaining pin inhibits distal movement of the striking assembly. In the second position, the retaining pin does not inhibit distal movement of the striking assembly. The actuator component includes a reloading channel. The actuator component is movable between a third position and a fourth position. In the third position, the retaining pin is in the first position and the retaining pin cannot be forced along the reloading channel. In the fourth position, the striking assembly can be used to move the retaining pin along the reloading channel.

Abstract: An apparatus for locating a central axis of a spinal column and method of using the same is disclosed. The apparatus and method includes one or more members capable of spanning a center line which may then be identified by at least one additional member positioned therebetween. Furthermore, the device may contain or be capable of accommodating various additional tools for marking the location of the central axis of a spinal column.

Abstract: A specimen retrieval apparatus includes a housing having an elongated tubular member extending distally therefrom. The elongated tubular member defines a longitudinal axis. An end effector assembly is coupled to a distal end of the elongated tubular member. The end effector assembly is configured to retain a specimen retrieval bag thereon. An articulation mechanism is operatively coupled to the elongated tubular member and the end effector assembly. The articulation mechanism is configured for selectively articulating the end effector assembly with respect to the longitudinal axis of the elongated tubular member.

Abstract: A system that breaks calcium in a liquid includes a catheter including first and second electrodes arranged to receive there-across a high electrical voltage at an initial low current. The high electrical voltage causes an electrical arc to form across the electrodes creating a gas bubble within the liquid, a high current to flow through the electrodes, and a mechanical shock wave. A power source provides the electrodes with the high electrical voltage at the initial current and terminates the high electrical voltage in response to the high current flow through the electrodes.

Abstract: Apparatus for controlling a steerable invasive probe having a handle. The apparatus includes a platform and a jig, which is mounted on the platform and is configured to receive the handle. The jig includes at least a first gear that is positioned and shaped to rotate the handle about an axis of the probe and a second gear that is positioned and shaped to operate a control on the handle for deflecting a tip of the probe. A drive module includes one or more motors. A transmission is coupled to the drive module and to the jig so as to controllably rotate at least the first and second gears and to translate the platform along a direction parallel to the axis in order to advance and retract the probe.

Abstract: A method and device for the extraction of follicular units from a donor area on a patient. The method includes aligning a dissecting punch over a follicular unit and rotating the dissecting punch to score the epidermis layer of the skin so that hair follicles are disposed within the lumen. The dissecting punch is then moved through the dermis layer and fatty tissue layer of the skin to dissect the follicular unit from the tissue surrounding the follicular unit.

Abstract: A device includes a clip including first and second arms distal ends of which are biased apart and a core member including first and second portions connected to one another via a frangible link. The first portion includes a first protrusion for engaging a cut-out in the first arm. The frangible link is fractured when subjected to a load of at least a predetermined level deploying the clip. The device also includes a capsule slidably housing the core member and a proximal portion of the clip.

Abstract: A device and method of promoting tissue adhesion to reinforce tissue apposition that may include collecting advancing a tissue apposition device to a body cavity having cavity calls, collecting tissue from the cavity walls, passing at least one tissue securement device through the tissue, applying energy to the collected tissue to produce injury to the tissue, and apposing the collected tissue and securing the one or more tissue securement devices. In this illustrative embodiment, the device and method promotes tissue adhesion between one or more portions of tissue, wherein the tissue adhesion may reinforce a tissue apposition.

Abstract: A surgical knot setter includes an elongated shaft having a long axis and proximal and distal portions. A tip is provided at the distal end of the shaft. The tip has a loop with an interior loop opening and a gate opening for permitting ingress and egress of a suture into the loop opening. The loop is laterally offset from the long axis and distal to the distal end of the shaft, such that the loop is laterally and longitudinally offset from the distal end of the shaft. A closure is provided for selectively opening and closing the gate opening between open and closed positions to selectively permit or prevent the suture from passing through the gate opening. An actuator moves the closure between the open and closed positions. A method for tying suture knots is also disclosed.

Abstract: A system for supporting the urethra using an introducer needle, the ends of which are flattened and which have openings therethrough, a handle having a latch mechanism which engages the opening in the flattened portion of the first end of the introducer needle, an implant, and a connector joining the end of the implant to the flattened portion of one of the ends of the introducer needle. These components are used to draw the implant into position, either through vaginal or abdominal incisions, to form a U-shaped loop beneath the urethra. The ends of the implant are adjusted to provide proper support for the urethra. The implant can have slits that open under applied tensile force.

Abstract: Novel deployment devices for use as adjuncts with tissue repair implants. The devices are removeably mounted to mesh tissue repair implant devices to manipulate the devices into position and provide for secure fixation about the periphery of such mesh implant devices by providing guide structures such as grooves for directing and positioning a surgical tacking instrument.

Abstract: An implant delivery system for delivering a sheet-like implant is disclosed. The device includes an implant spreader assembly disposed proximate the distal end of a delivery shaft. The implant spreader assembly includes a first arm and a second arm. The arms are coupled to the delivery shaft such that the first arm and second arm are moveable between a closed position and an open position. When the first and second arms are in the closed position, the arms extend generally in the longitudinal direction. When pivoting to the open position the distal end of each arm travels in a generally transverse direction to spread a sheet-like implant.

Abstract: This disclosure is directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Further rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque.

Abstract: A fluid ejection device includes a pulsating flow generation section adapted to eject a fluid in a pulsed manner; a fluid supply section adapted to supply the pulsating flow generation section with the fluid; a fluid supply tube having flexibility adapted to communicate the pulsating flow generation section and the fluid supply section with each other; and a drive control section adapted to perform drive control of the pulsating flow generation section and the fluid supply section, wherein the drive control section starts up the pulsating flow generation section, makes the fluid supply section supply the fluid at a first flow rate for a predetermined time period, and then makes the fluid supply section supply the fluid at a second flow rate lower than the first flow rate after the predetermined time period elapses.

Abstract: A fluid ejection device includes: a fluid chamber; a volume varying unit configured to vary the volume of the fluid chamber; a fluid supplying unit configured to supply fluid to the fluid chamber at a predetermined pressure; and an ejection command switching unit configured to switch a fluid ejection between a pulsed flow ejection which ejects the fluid in a pulsed manner by activating the volume varying unit and varying the volume of the fluid chamber and a continuous flow ejection which ejects the fluid with a fluid supply pressure from the fluid supplying unit higher than that in the case of the pulsed flow ejection in a state in which the volume varying unit is stopped.

Abstract: Vitrectomy probes and system related thereto are disclosed herein. The disclosure describes various example vitrectomy probes having an adjustable cutting port size. Various example features are described for adjusting the size of the cutting port. Further, the disclosure provides examples for adjusting the size of the cutter port while the vitrectomy probe is in operation.

Abstract: A dermatological skin treatment device is provided. The device comprises a handpiece and a cutting tool, wherein the tool is inserted through the conduit and percutaneously inserted into a tissue disposed within a recessed area of the handpiece. The device and method cut the fibrous structures under the skin that cause cellulite at an angle substantially parallel to the surface of the skin and replace these structures with a non-cellulite forming structure by deploying a highly fibrous mesh through a single needle hole to create a highly fibrous layer directly or through wound healing processes.

Abstract: A surgical cutting and fastening instrument that is motorized. The instrument comprises in one embodiment a charge accumulator device, separate from a battery, that provides additional power to the motor under certain conditions. In addition, the motor may comprise multiple windings.

Abstract: An improved safe and convenient disposable automatic lancet, comprising a housing (1), a needle core (2), a spring (3) and a protective rod (4), wherein, a pressing arm of a trigger button (10) is divided into a first pressing leg (11) and a second pressing leg (19), and the first pressing leg (11) is used for triggering an elastic arm in a locking structure to form a press-type trigger structure, and the second pressing leg (19) fits with a safety sleeve (20) and a press-down channel (17) to achieve a safety function of the trigger button (10); a barb (12) on the second pressing leg (19) fits with a self-locking hook (13) on the housing (1) so as to achieve a self-locking function after one press. In order to shorten the exposed needle length of a needle body on the needle core (2), in the automatic lancet, the distance between the second pressing leg (19) and the needle tip (7) is designed to be less than the distance between the first pressing leg (11) and the needle tip (7).

Abstract: A lancing system comprising a lancet with a handle portion and a needle bearing portion, the needle bearing portion retaining a thin needle protected by a safety cap. The safety cap includes first and second chambers, where the first chamber acts as a sheath and the second chamber having a surface positioned to compromise the structure of the needle when the needle bearing portion of the lancet body is inserted into the second chamber.

Abstract: A lancet device including a housing and a lancet structure having a puncturing element. The lancet structure disposed within the housing and adapted for movement between a retaining or pre-actuated position wherein the puncturing element is retained within the housing, and a puncturing position wherein the puncturing element extends through a forward end of the housing. The lancet device includes a drive spring disposed within the housing for biasing the lancet structure toward the puncturing position, and a retaining hub retaining the lancet structure in the retracted position against the bias of the drive spring. The retaining hub includes a pivotal lever in interference engagement with the lancet structure. An actuator within the housing pivots the lever, thereby moving the lancet structure toward the rearward end of the housing to at least partially compress the drive spring, and releasing the lever from interference engagement with the lancet structure.

Abstract: A vascular occlusion device for occluding a body cavity includes an elongate member for injecting embolization material into the body cavity and a deflecting device. The deflecting device is disposed around a distal end of the elongate member and is expandable to contact an interior wall of the body cavity in the expanded state. The deflecting device is configured to be deflected by the embolization material to change a shape of the deflecting device in the expanded state. The deflecting device provides a visual and tactile indication of completion of embolization based on the shape of the deflecting device in the expanded state.

Abstract: Non-expandable space-occupying devices for treating voids within the body are disclosed. The devices can have multiple non-expandable space-occupying elements connected to a flexible leaden. Methods of making and using the devices are also disclosed.

Abstract: A distal protection device provided with a filter basket having a self-expanding radial loop designed to position the filter basket within human vasculature and to hold the filter basket open during deployment.

Abstract: A clot removal device and method for removing a clot from a blood vessel may employ a tubular clot capture element. The clot capture element may be configured for deployment in a blood vessel for surrounding a clot. The clot capture element may have an opening therein configured to receive and guide a clot engaging element and may be configured to radially contract upon retraction, such that when the clot capture element surrounds a clot and is retracted in a longitudinal direction of the blood vessel, the clot capture element is configured to exert a radially inward compression force on the clot.

Abstract: According to an aspect of the present disclosure, an endoscopic surgical device is provided and includes a handle assembly; a tube assembly operatively supported on and extending from the handle assembly, the tube assembly defining a longitudinal axis; an articulation assembly operatively supported on and extending from a distal end of the tube assembly; and a tool assembly operatively supported on and extending from a distal end of the articulation assembly. In use, a rotation of the handle assembly about the longitudinal axis results in a concomitant rotation of the tool assembly; an actuation of the handle assembly in a particular manner results in a concomitant actuation of the tool assembly; and a pivoting of the handle assembly in any off-axis direction relative to the longitudinal axis results in a concomitant articulation of the tool assembly via the articulation assembly.

Abstract: The invention relates to a medical instrument comprising at least one movable tool element and at least one actuating element which is mounted such as to be pivotal about a pivotal axis and is coupled to the at least one tool element for the purposes of moving the tool element as a result of a pivotal movement of the actuating element, wherein, for the pivotal mounting of the at least one actuating element, there is provided a pivotal bearing comprising a bearing shaft holder and a bearing shaft which is held in the bearing shaft holder in a working position, wherein the at least one actuating element incorporates the bearing shaft or the bearing shaft holder, wherein the bearing shaft holder has an insertion opening and is insertable through the insertion opening into the bearing shaft holder in a direction that is transverse or substantially transverse to the pivotal axis.

Abstract: A medical device and method for closure of a puncture in a body lumen are disclosed. The device has an aggregate (10) of a support structure (20) and a substantially fluid tight patch member (30) attached thereto at an attachment unit (40). The aggregate has a first, temporary delivery shape, for delivery to an interior of said body lumen and to be subsequently subjected to a change of shape to a second shape, which is a tubular shape. When delivered in said body lumen, the patch member is arranged radially outside of said tubular support structure and arranged towards an inner tissue wall of the body lumen. The aggregate is the detached from a delivery device and said puncture is intraluminally closed in a leakage tight manner, advantageously supported by a physiological pressure of a body fluid in said body lumen. The device may biodegrade over time.

Abstract: The present invention generally relates to devices and methods for reversibly coupling an implant to a deployment device.