Abstract: A suturing device for grasping soft tissue and placing stitches in soft tissue during endoscopic procedures is described. An elongate housing with a stationary jaw and a movable jaw disposed at the distal end are configured for grasping and releasing soft tissue. A movable needle disposed within the housing is actuated to engage a length of suture and drive the suture into and through the grasped soft tissue. A suture capture member is disposed on the movable jaw and is configured to allow passage of the needle therethrough while securing a portion of the stitched length of suture.

Abstract: Suture passer devices, including suture passers configured with an axially slideable jaw that includes a tissue-penetrating distal end region. Also described are suture passers including jaws housing tissue penetrating needles to pass suture that are substantially thin. Methods of using such devices to pass a suture through tissue are provided.

Abstract: In various embodiments, a compensator can comprise a compensator body comprising a plurality of first packets and a plurality of second packets wherein, in at least one embodiment, each second packet is positioned intermediate two or more first packets. The compensator can further comprise a first medicament positioned within each first packet and a second medicament positioned within each second packet, wherein the first medicament is different than the second medicament.

Abstract: A stapling system for use with a surgical stapling instrument is disclosed. The stapling system comprises a staple cartridge, a staple cartridge carrier, and a first articulation joint defining a first articulation axis. The stapling system further comprises a second articulation joint defining a second articulation axis, an elongate shaft, and a shaft portion extending between the first articulation joint and the second articulation joint, wherein the shaft portion is pivotable relative to the elongate shaft about the second articulation axis. The stapling system further comprises, one, means for articulating the staple cartridge carrier about the first articulation axis and, two, a drive member operably supported with the staple cartridge carrier, wherein the drive member is selectively operable to eject staples from the staple cartridge.

Abstract: In various forms, the access devices form at least one passageway through which various surgical instruments and tools may be admitted into the body cavity. Various embodiments may be configured to support an anvil for a circular stapling device therein. Various forms employ a flexible bag for retrieval of specimen from the body cavity.

Abstract: An intraluminal occlusion device includes a frame and an attached covering. The frame includes longitudinal struts having concave and convex portions. The intraluminal occlusion devices can be implanted at an opening to a body vessel, such as a blind passage, to block the entry of fluid into the vessel. Methods of blocking the entry of fluid into bodily passages are also described.

Abstract: An occlusive device for left atrial appendage occlusion that has a membrane component configured to inhibit passage of blood and an expandable frame formed from a plurality of wires having a cupped occlusive component at least partially covered with the membrane component, one or more anchors with looped ends and a hub component. The occlusive device can be delivered percutaneously. The occlusive device is useful in the occlusion of the left atrial appendage.

Abstract: A clip applier includes a shaft having a proximal end and a distal end. Further, the distal end of the shaft includes a flexible tool having at least two rails connected to each other by at least one jointed connection, and the at least two rails configured to rotate about the jointed connection. Additionally, a pair of jaws may be provided at a distal end of the flexible tool. Further, an actuator may be provided at the proximal end of the shaft to advance the surgical clip within the flexible tool.

Abstract: Embodiments of apparatuses and methods for microfracture (e.g., forming a plurality of microfractures in a bone to encourage cartilage regeneration).

Abstract: An orthopaedic surgical instrument comprising an internal support about which a plastic substrate is disposed, and which includes exposed cutting surfaces relative to the plastic substrate. The surgical instrument may have a generally hemispherical shape and the internal support may comprise a non-planar shim. In particular embodiments the shim includes multiple interconnected limbs with multiple holes or slots disposed in the limbs and with the holes or slots including the cutting surfaces.

Abstract: Devices and methods for use in hip replacement surgery can incorporate computer models of a patient's acetabulum and surrounding bone structure, a first patient-specific jig designed from the computer model and configured to correspond to a final installation position and orientation of a prosthetic hip implant, a second patient-specific jig, also designed from the computer model, configured to refine the procedure, if necessary, following use of the first patient-specific jig, and/or a third patient specific jig, designed from the computer model, configured to refine the procedure, if necessary, following use of the first and second patient-specific jigs, allowing the surgeon to properly position and orient the hip prosthesis. Also shown and described are novel devices for implanting an acetabular cup.

Abstract: An implant for use in high tibial osteotomy can include a central implant portion, a first side implant portion and a second side implant portion. The first and second side implant portions can be selectively rotatable relative to each other. A method of performing high tibial osteotomy can include providing an implant having a superior surface and an inferior surface. The first superior surface and the second inferior surface can define an implant angle therebetween. A correction angle of the tibia can be determined. A first cut can be made in the tibia. An angle of a second cut relative to the first cut can be determined based on a difference between the implant angle and the correction angle. The second cut can be made in the tibia. The tibia can be opened creating an opening for receipt of the implant. The implant can be inserted into the opening.

Abstract: A tissue-separating catheter assembly comprises a rotatable shaft, having a distal shaft portion, and a tissue separator device extending along the shaft. The tissue separator device has a distal separator part at the distal shaft portion movable between a retracted state, towards the distal shaft portion, and an outwardly extending, operational state, away from the distal shaft portion. A pivot joint may be used to pivotally connect the distal separator end to the distal shaft portion. The distal shaft portion may comprise a distally-facing transition surface at a proximal end of the distal shaft portion. First and second energizable tissue separator elements may be used at the transition surface and the tip of the device, respectively.

Abstract: The invention relates to an instrument for treating biological tissue, including a housing, in which is disposed a ballistic device for generating extracorporeal shock wave-like pressure waves and a transfer element permanently placed on the biological tissue, said element coupling the pressure waves into the body of living creatures, wherein the transfer element couples non-focused, ballistically generated, shock wave-like pressure waves into the biological tissue, the waves generated by a striking member that is accelerated to a high final velocity of over 5 m/s by a pneumatic medium which is under an operating pressure in a pressure channel. A quick-acting valve releases the pneumatic medium, which is under working pressure, into the pressure channel, wherein a control circuit controls the duration of opening of the valve as a function of at least one or a combination of the following parameters: working pressure, impact frequency or pressure in the back-pressure chamber.

Abstract: An obstruction removal device is described, having one or more engaging members which can engage portions of the clot. The one or more engaging members have a collapsed, delivery state, and an expanded, deployed state.

Abstract: A surgical guide to facilitate delivery of a therapy delivery device into the pterygopalatine fossa of a subject includes a curvilinear body having a distal end portion, a proximal end portion, and an intermediate portion extending between the distal and proximal end portions. The proximal end portion is defined by oppositely disposed first and second surfaces. The proximal end portion and the intermediate portion define a longitudinal plane that extends between the proximal and distal end portions. The distal end portion has an arcuate configuration relative to the longitudinal plane and is defined by oppositely disposed third and fourth surfaces.

Abstract: An articulating laparoscopic instrument including a handle, an outer shaft, an end effector, and a wrist assembly. The wrist assembly connects the end effector to the shaft and includes torque and articulation mechanisms. The torque mechanism includes a plurality of links disposed over the rod and connected with one another in a pivotable yet rotationally locked fashion. The articulation mechanism includes a plurality of articulation member disposed over the rod to collectively define a deflection section. The links freely rotate relative to the articulation members, with the rod and links collectively bending in response to a change in shape of the deflection section.

Abstract: An endoscopic instrument includes a rigid hollow shank (2) and a tool (8) at the distal instrument end. The tool (8) is driven in rotation via a drive shaft (14), which is guided within the hollow shank (2). At the distal end of the hollow shank (2), the tool (8) projects out of the hollow shank (2), where it may be angled with respect to the distal end of the hollow shank (2).

Abstract: An endoscopic surgical device comprising a slotted clear cannula, a blade and a housing, wherein the cannula is attached to the housing, and wherein the blade is enclosed in the housing and is slidable into the cannula is disclosed. The blade is enclosed within the housing and cannula, and has a horizontally-oriented pushing component and a vertically-oriented cutting component that protrudes through the slot of the cannula. A method for a performing an operative procedure on a target tissue in a subject using the endoscopic surgical device is also described.

Abstract: An ultrasonic surgical blade has a blade body at a distal end and a shank at a proximal end, the shank being connectable at a proximal end to a source of ultrasonic mechanical vibrations. A sheath surround at least a portion of the shank. The sheath is configured to define a space between an outer surface of the shank and an inner surface of the sheath. The shank is provided with a liquid-conducting channel terminating in at least one outlet at the outer surface of the shank to enable delivery of irrigant to the space between the shank and the sheath for eventual conduction along an outer surface of the blade body.

Abstract: A rotational atherectomy device for removing a stenotic tissue from the iliac artery of a patient. The device comprises a flexible, rotatable drive shaft having an elongated proximal portion, an elongated distal portion, and an abrasive element mounted to the drive shaft between the elongated proximal and distal portions of the drive shaft and configured for rapid rotation together with the drive shaft. The drive shaft is configured to extend throughout an entire length of the iliac artery to be treated and one elongated portion of the drive shaft extends out of the patient through a first access opening located in a femoral artery which is ipsilateral to the treated artery. Another elongated portion of the drive shaft extends through a second access opening located in another peripheral artery of the patient.

Abstract: The devices and methods shown provide for the minimization of extravasation during arthroscopic surgery. The anti-extravasation surgical portal plug allows a surgeon to drain excess fluids from the soft tissue surrounding the surgical field during arthroscopic surgical procedures.

Abstract: In one form, a system for use in percutaneous surgical procedures includes a cannula having an elongate body extending along a longitudinal axis between a proximal end and a distal end and including a working channel dynamically expandable from a first, unexpanded configuration. The system also includes a device that is positionable in and engageable with the working channel to expand the working channel from the first configuration as the device is moved through the working channel. In response to disengagement of the device with the working channel, the working channel returns to the first, unexpanded configuration. In one aspect of this form, the device includes an interbody spinal implant that is deliverable to a surgical site through the working channel of the cannula. In another form, a method for performing a percutaneous surgical procedure is provided. However, different forms and applications are envisioned.

Abstract: The present invention discloses a vaginal manipulator configured to be inserted through a vaginal opening. The vaginal manipulator includes an elongated portion having a proximal end portion and a distal end portion. The elongated portion has an actuating mechanism. The vaginal manipulator further includes a head portion extending from the distal end portion of the elongated portion. The head portion includes a linear piercing member. The piercing member is configured to temporarily help retain a bodily implant proximate an outer surface of a vaginal wall. The piercing member is configured to move from a retracted position to an extended position with respect to the head portion. Further, the actuating mechanism is operatively coupled to the piercing member and is configured to move the piercing member from its retracted position to its extended position.

Abstract: A system for flexibly stabilizing a vertebral motion segment by connecting a first vertebra and a second vertebra is disclosed. The system includes an elongate connection element with end portions interconnected by a flexible coupling member. The system includes first and second attachment portions for connecting the connection element to the vertebrae. A first resilient member is positioned between the first end portion and the first attachment portion, and a second resilient member is positioned between the first attachment portion and the second attachment portion. The system is designed such that the second resilient member is compressed when the first and second attachment portions move towards each other, and the first resilient member is compressed when the first and second attachment portions extend away from each other.

Abstract: The present teachings provide one or more surgical implements for repairing damaged tissue, such as in the case of a spinal fixation procedure. A uniplanar bone anchor system for a fixation procedure is provided. The system can include a bone fastener including a head with a bearing surface and a shaft adapted to engage an anatomy. The system can also include a saddle, which can include a first bore formed about a longitudinal axis that receives the bone fastener and a coupling bore defined transverse to the longitudinal axis. The system can also include a coupling system, which can have a second bearing surface. The coupling system can be received through the coupling bore such that the second bearing surface of the coupling system can contact the bearing surface to permit the bone fastener to move in only one plane.

Abstract: A surgical connector useful to link spine rods together. The connector may be used adjacent a pair of mounting screws in one vertebra to limit movement between the screws or may be used to apply a lateral force to a portion of the spine to change curvature. A method of performing spinal surgery is also provide to reinforce a patient's spine.

Abstract: Devices and corresponding methods for the correction of spinal column deformities, vertebral displacements and for the surgical fixation of the spine including vertebral fixing element(s), vertebral connector element(s), and polyaxial correcting element(s) that can house along its structure varying specifically oriented correction element(s). The polyaxial correcting element(s) are mobilized with the help of correcting force element(s) that induce a three-dimensional mobilization of the polyaxial correcting elements and the vertebrae to which these are attached. Longitudinal spinal fixing element(s) provide for the definitive fixation of the spine. The longitudinal spinal fixing element(s) are joined and fixed to the vertebral fixing element(s) or to permanent vertebral connector element(s).

Abstract: Devices, systems and methods for dynamically stabilizing the spine are provided. The devices include an expandable spacer or member having an unexpanded configuration and an expanded configuration, wherein the expandable member in an expanded configuration has a size, volume and/or shape configured for positioning between the spinous processes of adjacent vertebrae in order to distract the vertebrae relative to each other. The systems include one or more expandable members and a mechanical actuation means for expanding the expandable member or an expansion medium for injection within or for filling the interior of the expandable member via the port. The methods involve the implantation of one or more devices or expandable spacers.

Abstract: A bone plate assembly including at least one bone plate, polyaxially adjustable fixation elements and a polyaxially adjustable locking mechanism. A first plate includes at least one polyaxial element for lockable connection with a fixation pad, and a connection feature which allows the plate to translate and polyaxially rotate relative to the locking mechanism. A second plate includes at least one polyaxial element for connection with a fixation pad and a connection feature for non-rotatable connection with the locking mechanism. The locking mechanism allows translation and polyaxial adjustment of the first plate relative to the second plate and locks the first and second plates via a taper lock. The fixation pad includes a deflectable spacer configured to prevent premature locking of the pad. Methods for implantation of the bone plate assembly between two bone structures are disclosed. Instrumentation for implantation, compression and locking of the bone plate assembly is disclosed.

Abstract: A bone plate system for use in an “open door” laminoplasty procedure, including a bone plate, a first fixation element, and at least one second fixation element. The bone plate is elongated and has a generally curved shape such that the plate has an associated radius of curvature. The plate is sized and dimensioned to span a gap between a pair of bony segments, for example a pair of bony segments constituting a divided lamina. The first and second fixation elements are each configured to securely attach the bone plate to the bony segments. The bone plate has a first end including a generally U-shaped slot extending therein such that the open end of the slot comprises a first terminal end of the plate.

Abstract: The present invention relates to a surgical apparatus for the implantation of a spinal column stabilization system generally, and more specifically to a surgical apparatus for the implantation of a spinal column stabilization system, which spinal column stabilization system comprises at least two bone screws which are respectively anchorable in a vertebra of a spinal column and which respectively comprise at least one first connecting element seating, and at least one connecting element which corresponds to the first connecting element seating and is insertable and fixable therein, wherein the apparatus comprises at least one multi-function sleeve having a proximal and a distal end, which multi-function sleeve defines a longitudinal axis and comprises a connecting element coupling device, a spreading-device coupling device and a holding instrument coupling device.

Abstract: A tool set for implanting a rod in a human spine in conjunction with bone screws includes a pair of end guide tools that receive opposite ends of the rod in channels and under manipulation by a surgeon facilitate transport of the rod toward the bone screws attached to the guide tools. Each end guide tool includes a laterally extending, rigid, rod holding structure located near a bottom surface thereof. Intermediate guide tools having pass-through slots are utilized to guide the rod to the bone screws at intermediate locations. For bone screw implantation, the end guide tools and intermediate guide tools are assembled with a driver. The driver is coaxial with the respective guide tool and rotatingly mateable thereto. The driver includes a stem and a nut-type fastener, the stem receivable in the guide tool. The fastener allows for rotation of the bone screw without rotating the attached guide tool.

Abstract: The present invention relates to a bone plating system and method for fracture fixation of bone. The bone plating system includes a bone plate, at least one locking screw, and at least one non-locking screw. The bone plate has locking holes with threads and non-locking holes. The locking screws have a shaft with a thread for engaging bone and a head with a thread configured and dimensioned to mate with the thread of the locking holes. The non-locking screws have a thread for engaging bone and a non-threaded head. Both the locking and non-locking screws remain seated in their respective holes for substantially as long as the bone plate is implanted. The non-locking screws compress the bone plate against the bone and hold fracture reduction while the locking screws are secured to the plate at a fixed angular relationship. The mixed fixation achieved by this bone plating system and method is particularly useful for treatment of per-articular fractures.

Abstract: An instrument for holding a bone plate may include a first arm, a second arm connected to and adjustable relative to the first arm, a first connection tip at the distal end of the first arm configured to connect to the first side wall of the bone plate, and a second connection tip at the distal end of the second arm configured to connect to the second side wall of the bone plate. A stabilizing member is connected to the first connection tip. The stabilizing member is distally spaced apart from the first connection tip to form an opening for receiving a portion of bone between the first connection tip and the stabilizing member.

Abstract: A method of compacting and stabilizing bone in the spine using an expandable screw and bone filler. The method includes placing an expanding screw through a pedicle and into a fractured vertebral body using established techniques; and expanding the screw within the body to create a cavity by tamping bone around the expanded aspect of the screw. The screw can be expanded and rotated about its rotational-axis to tamp bone adjacent to the expanded screw. After compaction, the screw is removed and the cavity is filled with bone filler.

Abstract: The invention relates to a method of treating obesity, insulin resistance and co-morbidities of these conditions by removing tissue from the abdomen. More specifically, it relates to a method of removing abdominal fat and omentum to which the fat is attached, in order to improve health.

Abstract: Systems and methods for non-thermal ablation of tissue are provided. A non-implantable minimally invasive system for treatment of tissue in a body via direct current ablation is provided including a catheter, a plurality of electrodes for deployment through the catheter, a power source for applying power to the electrodes, and a fixation element for maintaining the catheter in a treatment position during treatment of the tissue. A minimally invasive method for treating tissue in a body via direct current ablation is provided including inserting a catheter into the body such that a portion of the catheter remains outside of the body, deploying a fixation element to fix the catheter in a treatment position, deploying a plurality of electrodes through the catheter, applying power to the plurality of electrodes, using the electrodes to apply a current to the tissue, and removing the catheter from the body.

Abstract: A system for performing mapping and ablation functions includes a catheter sized and shaped for vascular access. The catheter includes an elongate body extending between a proximal end and a distal end and having at least one inner fluid lumen. The catheter further includes a tip section positioned proximate to the distal end of the body. The tip section includes a proximal portion and a distal portion. The distal portion can have a distal end that can be substantially planar. The system also includes one or more electrode structures exposed at the tip section such that the one or more electrode structures disposed proximate the substantially planar distal end of the tip section.

Abstract: Image-guided therapy of a tissue can utilize magnetic resonance imaging (MRI) or another medical imaging device to guide an instrument within the tissue. A workstation can actuate movement of the instrument via a probe driver, and can actuate energy emission and/or cooling of the instrument to effect treatment to the tissue. The workstation and/or an operator of the workstation can be located outside a vicinity of an MRI device or other medical imaging device, and drive means for positioning the instrument can be located within the vicinity of the MRI device or the other medical imaging device. The instrument can be an MRI compatible laser probe that provides thermal therapy to, e.g., a tissue in a brain of a patient. The probe driver allows for precise positioning, stabilization and manipulation of a probe.

Abstract: A novel collection device for collection, storage and disposal of biological products, in conjunction with an improved cleansing method. Disclosed is an apparatus which includes a locking closing member handle to allow for safe transport and disposal of medical waste. Closing member allows for secure containment of medical waste and subsequent apparatus cleaning. Closing member design includes a gap between closing member and housing which facilitates device cleaning after waste disposal.

Abstract: Surgical devices are disclosed herein that generally include an intracorporeal elbow joint to facilitate translational movement of an end effector while allowing a body portion of the surgical device and a trocar or working channel through which the device is inserted to be maintained in a fixed angular orientation relative to the patient. This allows a plurality of such devices to be used effectively with a single incision or access device. Such devices also generally provide end effector movement with six degrees of freedom, while maintaining a mechanical linkage between the user and the end effector and while mimicking and/or mirroring natural user movement. Various methods related to such devices are also disclosed.

Abstract: A system for remotely controlling the positioning within the body of a patient of an elongated medical device optionally having a control handle, comprises a catheter position system and a remote controller configured to control the robotic device. The catheter position system includes a handle controller; a sled member coupled to the handle controller, the sled member being configured to position the medical device within the body of the patient; and a sled base configured to advance the sled member towards the body of a patient, the sled bed being coupled to a sterile barrier effective to maintain sterility inside the sled base. The catheter position system may include a control system configured to issue positioning commands in response to sensor signals received from the catheter. The catheter position system may also include a motor driven rotatable catheter introducer clamp configured to enable rotation of an introducer.

Abstract: Apparatus, systems and methods for associating medical diagnostic and treatment probes with connection ports of a multiport instrument console. Proximity sensing between a probe and the console provide user-detectable signals indicating the availability or nonavailability of a compatibly configured port for the probe, and specific identification of one or more ports that are compatible with the probe. The proximity sensing also provides capability for identifying and configuring a probe before attempting to connect the probe to a console port.

Abstract: A visualization device for use with a loading tray includes a frame comprising a floor, a first side wall extending generally perpendicular from the floor, and a second side wall extending generally perpendicular from the floor and spaced from the first side wall. The visualization device further includes a mirror abutting the floor of the frame. A magnifying glass may also be supported by top edges of the first and second side walls, or by runners coupled to the top edges of the first and second side walls. The visualization device may be slideably disposed in a reservoir of a loading tray.

Abstract: Method and apparatus for the evacuation of intracerebral hematomas comprises a minimally invasive non-operating room surgical apparatus within a neuro-navigation system that can provide real-time imaging of the ICH evacuation procedure. Apparatus uses an auger housed within an apertured lumen which, when placed in proximity to a hematoma and rotated in an appropriate direction, causes the removal of the clotty material from the hematoma. Apparatus also includes ultrasonic imaging capability and an electromagnetic tracking coil to enable real-time, three-dimensional visualization of the evacuation procedure.

Abstract: A system is disclosed for determining a position and a change in the position of an anatomical structure. The system utilizes a surgical navigation system and a substrate that is capable of being removably mounted to an outer surface of a patient's body. The substrate includes a sensor that is tracked by the surgical navigation system and a positional device that determines the position of an anatomical structure relative to the sensor. The concatenation of the position of the sensor and the relative position of the anatomical structure allows a global position of the anatomical structure to be determined by a computer system and displayed to the user.

Abstract: In some aspects, methods can include providing a top loading dental surgical guide including a dental drill guide positioning ring housed within the template material, the positioning ring including a body defining an inner surface and a retention element extending inwardly from the inner surface; coupling the surgical guide to the region to be drilled; temporarily engaging a drill guide within the positioning ring by axially coupling using the retention element, independently of a rotational motion of the drill guide relative to the positioning ring by engaging the retention element within a complementary recessed feature of the drill guide; performing a drilling procedure with a drill guided by the drill guide; and disengaging and removing the drill guide from the positioning ring.

Abstract: Embodiments are provided for using an individualized orthodontic treatment index. One method embodiment includes receiving an initial virtual dental model from a first scan of a patient's dentition, modifying the initial virtual dental model to create a target virtual dental model according to a treatment goal, assigning a number of dental references to the target virtual dental model, receiving a treatment outcome virtual dental model from a second scan of the patient's dentition, mapping the number of dental references from the target virtual dental model to a treatment outcome virtual dental model, and calculating an individualized treatment index score for the treatment outcome virtual dental model according to one or more differences between the target virtual dental model and the treatment outcome virtual dental model based on the number of dental references.

Abstract: The present invention is a dental implant utilizing a polymeric dental post. The actual prosthetic portion of the implant may also be manufactured from a polymer. Various post designs are disclosed for setting and securing the post in a patient's jaw. Numerous polymers are disclosed and may be blended to achieve desired characteristics for both the post and prosthetic.