Abstract: The present disclosure relates to a method and a system for determining the fertility status of a female. The method comprises the steps of determining and recording a continuous series of temperature data points relating to a body temperature of the female, identifying if the series of temperature data points comprises at least one pre-determined feature in the series of temperature data points and, if a pre-determined feature has been identified, determining a point in time of ovulation for the series of temperatures based on a pre-determined relation of the pre-determined feature and ovulation.

Abstract: A system and method for enhanced navigation for use during a surgical procedure including planning a navigation path to a target using a first data set of computed tomography images previously acquired; navigating a marker placement device to the target using the navigation path; placing a plurality of markers in tissue proximate the target; acquiring a second data set of computed tomography images including the plurality of markers; planning a second navigation path to a second target using the second data set of computed tomography images; navigating a medical instrument to a second target; capturing fluoroscopic data of tissue proximate the target; and registering the fluoroscopic data to the second data set of computed tomography images based on marker position and orientation within the real-time fluoroscopic data and the second data set of computed tomography images.

Abstract: A powered medical device includes electronic components on a circuit board embedded within the body of a plug for connecting the device with a control apparatus. The medical device may be repaired or refurbished without the need to access the embedded circuit board through the use of a supplemental circuit board installed into the open end of the plug adjacent the plug pins. The supplemental circuit board may include a variety of electronic components, including fuses or non-volatile memory.

Abstract: A medical instrument including a shaft and an actuated structure mounted at a distal end of the shaft can employ a pair of tendons connected to the actuated structure, extending down the shaft, and respectively wound around a capstan in opposite directions. A passive preload system may maintain minimum tensions in the tendons.

Abstract: A treatment instrument includes a power receiver and a treatment section configured to be driven by power received by the power receiver. The power receiver includes a first solenoid-shaped power receiving coil and a second solenoid-shaped power receiving coil having a winding direction opposite to a winding direction of the first power receiving coil. The first power receiving coil and the second power receiving coil have the same length and the same number of turns, and are arranged concentrically. The first power receiving coil and the second power receiving coil are electrically connected to a treatment section so that a direction in which a current flows through the first power receiving coil is opposite to a direction in which a current flows through the second power receiving coil.

Abstract: A surgical instrument including a housing, an endoscopic portion, a shaft portion, and an end effector is disclosed. The endoscopic portion extends distally from the housing and defines a longitudinal axis. The shaft portion is selectively connectable to a distal end of the endoscopic portion. The end effector is selectively connectable to a distal end of the shaft portion.

Abstract: A surgical instrument for dispensing a fluid includes a housing and a dispensing shaft, which is elongate and which has a proximal end and a distal end. The proximal end of the dispensing shaft is received in the housing and the distal end defines a dispensing opening for dispensing the fluid. The dispensing shaft includes a through bore which extends along the dispensing shaft from the proximal end to the dispensing opening at the distal end. The instrument further includes a dispensing assembly and a priming assembly connected to the housing which is operable to move an amount of the fluid into the through bore of the dispensing shaft to prime the through bore with the fluid before the dispensing assembly is operated.

Abstract: An orthopedic distraction device is provides. The orthopedic distraction device includes a first upper paddle for engaging a first bone of a joint, a lower paddle for engaging a second bone of the joint and a displacement mechanism. The displacement mechanism includes a drive assembly operable to move the upper paddle relative to the lower paddle. The lower paddle is releasably connected to the displacement mechanism.

Abstract: A surgical instrument includes a body, a shaft, and a cartridge receiving assembly. The body has an actuator. The cartridge receiving assembly includes a first jaw and a second jaw. The first jaw is movable relative to the second jaw between an open position and a closed position. The first and second jaws are configured to receive a suture cartridge therebetween when the first jaw is in the open position. The first and second jaws are configured to secure a suture cartridge therebetween and thereby operatively couple the actuator with the suture cartridge when the first jaw is in the closed position. The first jaw is further configured to receive a needle of the suture cartridge directly thereagainst when the first jaw is in the closed position such that the first jaw is configured to capture the needle within the suture cartridge.

Abstract: A method for securing a strand to a fixation member for arthroscopic fixation, wherein the fixation member includes a channel on an exterior surface and an aperture therethrough. The method includes passing a strand having first and second ends through a flexible sleeve, passing the sleeve through the aperture of the fixation member in a first direction, tensioning the strand, and pulling the sleeve in a second direction different than the first direction to secure the sleeve to the fixation member without tying the strand on the fixation member.

Abstract: An apparatus is disclosed which comprises a handle module that is attachable to a detachable shaft module for collectively performing a surgical procedure and an inspection station for connection to the handle module when the handle module is not being used in a surgical procedure. The handle module comprises a handle module memory circuit for storing handle module usage data for the handle module. The inspection station comprises an inspection station processor circuit for determining one or more service recommendations for the handle module based on the handle module usage data stored in the memory of the handle module and based on service recommendation criteria.

Abstract: An apparatus for joining two hollow organ sections with an annular array of surgical staples includes a staple cartridge component, an anvil component, a buttress component and a fastening member. The staple cartridge component includes a plurality of surgical staples arranged in an annular array. The anvil component is movable relative to the staple cartridge component between spaced apart and approximated positions to adjustably clamp the organ sections between the staple cartridge and anvil components. The buttress component is configured and dimensioned to be positioned on a distal surface of the staple cartridge component. In particular, the buttress component includes a buttress member and a plurality of circumferentially arranged tabs extending proximally from the buttress member. The fastening member is configured and dimensioned to engage the plurality of circumferentially arranged tabs to securely position the buttress component on the staple cartridge component.

Abstract: A stapling assembly comprising an end effector movable from an open configuration to a closed configuration is disclosed. The end effector comprises an anvil and a staple cartridge comprising a first tissue-contact surface, a second tissue-contact surface stepped up from the first tissue-contact surface, an annular row of cavities, and a plurality of staples removably stored in the cavities. The anvil is configured to transition the staples from an unformed configuration to a formed configuration. Each staple comprises a crown, a first staple leg extending from the crown, and a second staple leg extending from the crown. The first staple leg and the second staple leg define a plane intersecting the crown in the unformed configuration. The first staple leg is bent toward a first side of the plane in the formed configuration. The second staple leg is bent toward a second side of the plane in the formed configuration.

Abstract: Transluminal access system includes a stent delivery catheter having a handle control mechanism. The catheter comprises a number of components for establishing an initial penetration between adjacent body lumens and subsequently implanting a stent or other luminal anchor therebetween. Manipulation of the stent components is achieved using control mechanisms on the handle while the handle is attached to an endoscope which provides access to a first body lumen.

Abstract: The cartridge assembly includes a housing, a pusher member, a fastener cartridge body, a circular cartridge buttress member, and a retaining ring member. The pusher member is supported within the housing and movable between a first position and a second position. The fastener cartridge body is supported on the housing and has a tissue engaging surface that extends to an annular edge. One or both of the housing and the fastener cartridge body define an annular containment groove. The circular cartridge buttress member has a body portion and an extension portion. The body portion is supported on the tissue engaging surface of the fastener cartridge body. The extension portion extends from the body portion and over the annular edge of the tissue engaging surface. The retaining ring member is secured within the containment groove to releasably secure the extension portion of the circular cartridge buttress member to the cartridge assembly.

Abstract: Medical device including an artificial contractile structure including at least one contractile element adapted to contract a hollow body organ, in such a way that the contractile element is adapted to be in a resting position or in an activated position, the activated position being defined with the contractile element constricting the hollow body organ and the resting position being defined with said contractile element not constricting the hollow body organ. The medical device can include a tensioning device adapted to apply a force so as to tighten the contractile element around said hollow body organ. The tensioning device can be arranged to cause the contractile element to apply a substantially uniform occlusive pressure of at most 8N/cm2, along the circumference of the contact area between the contractile element and the hollow body organ when the contractile element is in its activated position.

Abstract: A method includes inserting into a patient organ a catheter including a position sensor, a device and a handle. The position sensor is attached to a distal end of the catheter. The device is movable along the catheter. The handle includes a control for navigating the device along the catheter to a target location in the patient organ. Based on a location of the position sensor, a target position of the control on the handle that corresponds to the target location of the device is estimated. A marker is set to mark the target position of the control on the handle, and the device is navigated to the target location by setting the control to the marker.

Abstract: An occlusion device intended for blocking perivalvular leak channels that are found following heart valve implantation between the heart valve and the surrounding tissue. The occlusion device has a stent and a covering that is attached to the stent surface. A blocking fabric extends across the lumen of the stent to block blood flow. The stent pattern and wall structure provide for small radius of curvature bends to fill narrow channels that cause the perivalvular leaks.

Abstract: A vaso-occlusive treatment system includes a delivery assembly; and a vaso-occlusive device detachably coupled to the delivery assembly by a delivery assembly junction. The vaso-occlusive device includes a braided portion formed out of one or more composite wires, a coiled portion coupled to the braided portion, and an intra-device junction coupling the braided portion to the coiled portion. Each composite wire includes a core made from a core metallic material, and an external layer made from an external metallic material different from the core metallic material. One of the core and the external layer has a greater radiopacity and a lesser stiffness, respectively, than the other one of the core and the external layer.

Abstract: A tourniquet band is made of an elastic material and has a plush surface on one side and a series of hook fastener material patches on the reverse side. The woven structure includes a series of parallel elastic threads covered by a dense yet loosely coiled bundle of non-elastic threads. The non-elastic threads are oriented to form the plush surface while allowing the elastic core thread to elongate for applying pressure to a body part by elastic compression when the tourniquet is wrapped around the body part and secured by joining the hook material with the plush surface.

Abstract: Embodiments provide a tourniquet that may be used as a daily wear belt. A tourniquet belt may include an elongate belt having a first end and a second free end; a securing element coupled to the elongate belt at the first end of the elongate belt; and a separate tightening element coupled to the elongate belt, wherein the tightening element is selectively actuable to tighten or loosen the tourniquet belt.

Abstract: Methods for preparing a bone in surgery using an imaging system, a navigation system having a locating device, and a robotic system having a cutting tool. A cannula is guided into an incision to expand the incision and provide access to the bone so that the cutting tool is insertable through the cannula to remove material from the bone. An implant is insertable through the cannula to be placed in the bone.

Abstract: Described herein are specialized endoscopic drilling devices that may be readily powered by a conventional shaver handpiece and further may be utilized to secure a soft tissue graft to a boney surface. More particularly, the devices, systems and methods of the present invention enable the efficient and minimally invasive formation of off-axis sockets and/or tunnels in boney surfaces that may then serve as a site for graft placement by aperture and/or suspensory fixation means. As such, the present invention has particular applicability to the surgical repair and reconstruction of torn or ruptured tissues, such as ligaments and tendons, in the leg, knee and shoulder, for example.

Abstract: Use of measurement system and detection module with a burr instrument for surgical procedures. The measurement system may include sensors (e.g., displacement, acceleration, and/or force sensors) that may be utilized to detect potentially hazardous operation of the burr instrument. For example, when penetrating through the cortex of the bone the measurement system may be operated in a unicortical mode such that when the burr passes through the cortex of the bone, the instrument operating may be arrested to avoid damage to surrounding tissue. Moreover, the system may be utilized to detect a slip or sudden loss of contact of the burr instrument such that the instrument may be arrested to avoid damage to surrounding tissue. Furthermore, the burr instrument may have a predetermined ramp-up speed.

Abstract: Unicortical path detection for a measurement system for monitoring a depth of penetration of a working portion of an instrument in a bone of a patient. The unicortical detection may compare an average cortex thickness in a bicortical path to an actual measured depth of penetration. If the actual depth of penetration exceeds the average thickness, a unicortical path may be detected. Upon detection of a unicortical path, an alert may be provided and/or the instrument may be arrested upon subsequent breaching of the cortex.

Abstract: A position adjustment device having a tool holder is locked to at least two pins projecting from respective anterior facing locations near a distal end of a tibia of a patient. The position adjustment device is adjusted. The position adjustment device is locked with the tool holder at first coordinates in the proximal-distal and medial-lateral directions. The distal end of the tibia is resectioned with a tool positioned on the tool holder, while the tool holder is in the first coordinates in the proximal-distal and medial-lateral directions. The tool is removed from the tool holder. A tibia trial is placed on the resectioned tibia using the tool holder, while the tool holder is in the first coordinates in the proximal-distal and medial-lateral directions. The tibia trial has a size and shape of a tibial tray of an ankle replacement system.

Abstract: Medical devices performing diagnostic and/or treatment procedures, such as retrieving autogenous materials and/or foreign materials from a patient are disclosed. The medical device may comprise a handle, a shaft coupled to the handle, and a retrieval device movably disposed within a working channel of the shaft. The handle may include a steering mechanism for deflecting a deflect a distal end of the shaft and a control mechanism for translating the retrieval device within the working channel. The retrieval device may be integrated into the medical device.

Abstract: An apparatus and method for capturing material within a body lumen are disclosed. The apparatus includes a core wire extending from a proximal end to a distal tip, an actuator member defining a lumen for receiving at least a portion of the core wire, and a distal basket having a distal enclosed end fixed relative to the core wire and one or more elements extending from a proximal open end to a collar slidable on the core wire. The collar is slidable on the core wire within an interior of the distal basket such that, when the collar contacts the actuator member, the collar applies an inward force to direct the proximal open end of the distal basket radially inwardly.

Abstract: Catheter-delivered endovascular medical devices are described. The devices may include a pull wire connected to a proximal body and a distal body, which may be formed of a basket or other framework that has a plurality of cells. The distal body may move/articulate proximally relative to and toward the proximal body. Methods of using and making the devices are also described.

Abstract: Provided herein are devices and methods for anterior arytenoid adduction. The device may comprise a wire having a first end and a second end at opposite ends of a longitudinal axis, the wire forming a spiral along the longitudinal axis and having a double hook at the first end, a suture threaded through the spiral of the wire from the second end to the first end, the suture forming a turn at the first end and passing exterior to the spiral to the second end. The method may comprise advancing a suture and hook from the subject's anterior thyroid cartilage or cricothyroid membrane to the muscular process of the subject's arytenoid, attaching the hook to the muscular process, and applying tension to the suture to rotate the muscular process and adduct the arytenoid.

Abstract: Articulating mechanisms, link systems, and components thereof, useful for a variety of purposes including, but not limited to, the remote manipulation of instruments such as surgical or diagnostic instruments or tools, are provided. The link systems include links wherein torque can be transferred between at least two adjacent links while allowing for pivoting motion between the links. Mechanisms for preventing undesired lateral movement of links relative to one another are also provided.

Abstract: [Object] To enable to detect a force acting on a surgical instrument with a simpler configuration. [Solution] Provided is an information processing device including an acting force calculation unit that calculates, on a basis of a first detected value by a first force sensor provided on one side of a rod-shaped member, at least one of acting forces on a first point of action and a second point of action that differ from each other on an other side of the rod-shaped member.

Abstract: A cutting instrument comprising: an outer tube; an inner tube rotatably disposed within the outer tube; the inner tube comprising an opening having a leading edge and a trailing edge; and the outer tube comprising a window having a leading edge and a trailing edge; at least one of the leading edge of the opening, the trailing edge of the opening, the leading edge of the window and the trailing edge of the window comprising a canted edge; and the window of the outer tube being adapted to be completely blocked by the inner tube during a phase of the rotation of the inner tube within the outer tube.

Abstract: An ultrasonic instrument includes a body, an actuation assembly, a shaft assembly, and an ultrasonic blade. The body defines a longitudinal axis and is configured to receive an ultrasonic transducer. The actuation assembly includes at least one annular activation member and at least one circuit. The at least one annular activation member extends angularly about the body along a 360 degree angular range. The at least one annular activation member is configured to move laterally relative to the longitudinal axis of the body. The at least one circuit corresponds to the at least one annular activation member. The shaft assembly includes an acoustic waveguide. The ultrasonic blade is in acoustic communication with the acoustic waveguide. The at least one activation circuit is configured to activate the ultrasonic blade in response to lateral movement of the activation member relative to the longitudinal axis of the body.

Abstract: Prostate treatment using fluid stream to resect prostate tissue, thereby relieving symptoms of conditions such as BPH, prostatitis, and prostatic carcinoma. A device having a fluid delivery element is positioned within a lumen of the urethra within the prostate. A fluid stream is directed outwardly from the fluid delivery element toward a wall of the urethral lumen. The fluid delivery element is moved to scan the fluid stream over the wall to remove a volume of tissue surrounding the lumen. The fluid may be combined with therapeutically active substances or with substances that increase resection efficiency. Fluid force may be adjusted to provide selective tissue resection such that soft tissue is removed while harder tissue is left undamaged. In order to gain a working space within the urethra, another fluid may be introduced to insufflate the urethra in the region of treatment.

Abstract: A direct stream hydrodynamic catheter system is provided for the removal of thrombus, lesions and the like including provisions for the infusion of drugs, lysing fluids and the like into a blood vessel. Physician controlled powered direct fluid jet streams emanate from a fluid jet emanatory in the form of robust radially directed fluid jet streams to impinge upon and ablate difficult and strong thrombus and lesions within a blood vessel. Effluent aspiration is controlled by an exhaust regulator in the form of a roller pump, but effluent removal can be assistingly influenced by the fluid pressure associated with the radially directed fluid jet streams.

Abstract: Apparatus and methods are provided for performing a medical procedure using an introducer sheath and a plurality of valve hubs. The introducer sheath includes a lumen extending between proximal and distal portions and a hub on the proximal portion. Each valve hub includes a valve body including a plurality of ports. The valve hubs may include different numbers and/or configurations of ports to facilitate introducing multiple instruments simultaneously through the tubular member. Optionally, the kit may also include one or more dilators. Each valve hub and the dilator may include connectors for mating with connectors on the tubular member hub releasably coupling a selected valve hub or the dilator to the tubular member.

Abstract: An instrument access device 1 comprises a proximal member 25 for location externally of an opening into a body cavity. A first connector 20 extends between the proximal member 25 and a first instrument receiver 2. A second connector 21 extends between the proximal member and a second instrument receiver 3. Instrument seals can be housed in relatively rigid housings for added strength.

Abstract: A surgical device for treating shoulder dystocia having a first arm having a proximal portion, a distal portion and a first curved surface, a second arm having a proximal portion, a distal portion and a second curved surface and a shoulder engagement section positioned at least between the distal portion of the first and second arms and connecting the first and second arms. The engagement section has an atraumatic surface and is configured to contact and press down on the baby to reposition the baby upon manipulation of the first and second arms.

Abstract: Polyaxial pedicle screw with a head in the shape of a ball segment and with a threaded screw shank, wherein a hollow ball segment with a recess for receiving a rod-shaped connector is mounted in the head, in order to permit pivoting movements and rotation movements of the connector, wherein moreover, in the direction of the longitudinal axis of the threaded screw shank, the head in the shape of a ball segment has a cutout with an inner thread in which the rod-shaped connector can be moved in and out and, by means of the inner thread in the cutout, a grub screw can be introduced for blocking the hollow ball segment. According to the invention, a plastic buffer body is fitted in the hollow ball segment and is connected to a ram, wherein the ram has a head which engages in an associated annular groove in the plastic buffer body.

Abstract: A cannulated bone anchor assembly includes a bone anchor, a receiver member for receiving a spinal fixation element to be coupled to the bone anchor, and a closure mechanism to fix the spinal fixation element with respect to the receiver member. The bone anchor includes a distal shaft having a first threaded section distal to a proximal head, a second threaded section distal to and adjacent the first threaded section, and a third threaded section distal to and adjacent the second threaded section. The first threaded section having a constant major and minor diameter. The second threaded section having a tapering major and minor diameter. The third threaded section having a tapering major diameter and a constant minor diameter.

Abstract: Various exemplary methods and devices are provided for fixing bone anchors to bone. In general, the methods and devices can allow for a bone anchor to be fixed to a bone at a desired angle to a surface of the bone. In an exemplary embodiment, a bone anchor assembly is provided that includes a bone anchor configured to engage bone, a receiver member for seating a head of the bone anchor, and a compression member for securing the bone anchor at fixed angle with respect to the receiver member when the compression member is seated within the receiver member. Corresponding engagement features of the compression member and the receiver member can be engaged in a secured configuration to inhibit or prevent removal of the compression cap from the receiver member and optionally to substantially prevent longitudinal and/or rotational movement of the compression member with respect to the receiver member.

Abstract: Implant connectors and related methods are disclosed herein. In some embodiments, a connector can include a low-profile portion to facilitate use of the connector in surgical applications where space is limited. In some embodiments, a connector can include a biased rod-pusher to allow the connector to “snap” onto a rod and/or to “drag” against the rod, e.g., for provisional positioning of the connector prior to locking.

Abstract: Joint implants, such as joint implants used for placement in toes to treat hammertoe are described. More particularly, joint implants that include a proximal portion configured to be inserted into a first bone, a distal portion configured to be inserted into a second adjacent bone, and an elongated body positioned between the distal and distal portion is described. The elongated body can define a length and include at least one metal rod extending from the proximal portion to the distal portion and a porous mesh extending along at least a portion of the elongated body length. The porous mesh can be configured to allow for bony in-growth upon implantation, wherein the elongated body defines a generally square cross section and is configured to be inserted into drilled circular holes in the first and second hones. Methods of fusing two adjacent phalanges of a two are also described.

Abstract: An intramedullary bone fixation device is disclosed herein. The device includes a first longitudinally extending member, a second longitudinally extending member, and a coupling member. The first longitudinally extending member includes a connector end and a bone engagement end opposite the connector end. The second longitudinally extending member includes a connector end and a bone engagement end opposite the connector end. The coupling member is configured to engage the connector ends of the respective longitudinally extending members, thereby coupling the first longitudinally extending member to the second longitudinally extending member. The device may be provided in an kit form at least partially unassembled. The device may be delivered into a fracture and fully assembled within the fracture or adjacent bone via percutaneous or minimally invasive surgical procedures. The device, on account of its configuration and assembly, may be considered modular in some cases.

Abstract: Compression screw systems for stabilizing and/or compressing bones of the extremities, characterized by a compression screw component and a hook component. The hook component is received on the compression screw component in any rotational position relative to the compression screw component in order to orient the hook component relative to a bone or bones requiring stabilization and/or compression. The hook component includes an anti-rotation feature, while a configured flange thereof provides a hook that extends about and overhangs a part of the bone. The compression screw component and the hook component may include cooperating structures that allow the hook component to attach to the compression screw component or allow the compression screw component to self-orientate with respect to the hook component upon compressing engagement of the compression screw head with the hook component. The configured flange of the hook component may terminate with a single, double or multiple tined prong.

Abstract: A medical implant according to the present invention includes a substrate having a plurality of discrete connection portions. Each connection portion has a top surface, a bottom surface, and a through-opening extending between the top surface and the bottom surface. A connecting member extends between each connection portion and connects adjacent connecting portions to each other. At least one of the plurality of connection portions has a first width and at least one of the connecting members has a second width, different from the first width. An outer covering substantially encompasses the substrate. The outer covering extends around the through-openings and encompasses the connecting member.

Abstract: A midline retractor provides access for the placement of PARS screws and other surgical sites. A lower profile allows for better visualization of the patients anatomy and provides better access for surgical instruments. The retractor may include integrated lighting, such as fiber optic lighting or other suitable lighting. The blades of the retractor may include a textured profile, such as diamond plating, grooves, etching or any other desired textured treatment on the blades. The texture on the blades may keep tissue from migrating down the blades and may prevent the blades from slipping up and out of the patient. The PARS retractor may include a blade rotation locking mechanism and/or a blade toe feature that allows for ease of use and an adjustable blade toe. The retractor may also include a rack release that provides for free movement of the rack.

Abstract: An improved method of implanting a bone graft in a joint and tools for accomplishing the same is disclosed. The present invention relates generally to tools and methods useful for treating a sacroiliac joint. In one embodiment, the present invention is a method including the steps of: creating a first incision in the patient's skin proximal to the patient's sacroiliac joint; creating an incision in the patient's skin over the patient's ilium; inserting a first working channel into said first incision and spreading said sacroiliac joint with an inserted end of said first working channel; inserting a second working channel into said second incision and forming a hole in said ilium; creating a void in said sacroiliac joint; inserting a graft into said void; and inserting a joint fusing device into said ilium and said sacrum.

Abstract: The disclosure pertains to an intravascular catheter, comprising an elongate member having a proximal end and a distal end, a balloon having an interior surface, an exterior surface, a lumen defined by the interior surface and a cylindrical wall extending between the interior surface and the exterior surface, the cylindrical wall having a proximal end and a distal end, the balloon having a plurality of weeping windows disposed in the wall and able to pass an electric current between the interior surface and the exterior surface and wherein the balloon wall is otherwise electrically insulative, and an electrode disposed in the balloon. The intravascular system is suited for modulation of renal nerves, for example.