Abstract: A suturing and cutting apparatus for endoscopic surgery includes a body, a head portion, and a transmission mechanism, the head portion, is connected rotatably to a distal end of the body relative to the axial direction of the body by the transmission mechanism. The transmission mechanism includes an operating rod, a connecting assembly and a gear transmission mechanism. The connecting assembly includes a first conversion component which is set between the body and the head portion and can rotate relative to the axial direction of the body. The aspects disclosed herein allow and facilitate in the performance of the endoscopic surgery.

Abstract: In an aspect, an ultrasonic horn includes a proximal flange, a first cylindrical portion having a first diameter and positioned distal to the proximal flange, a second cylindrical portion including a second diameter and a distal end, in which the second cylindrical portion is at a position located distal to the first cylindrical portion and in which the second diameter is smaller than the first diameter, a tapered portion disposed between the first cylindrical portion and the second cylindrical portion, and a cylindrical mass disposed about the horn at a position located between the flange and the distal end of the second cylindrical portion. In another aspect, an ultrasonic system comprising an end-bell, an ultrasonic horn as disclosed above, a transducer portion disposed between the end-bell and the ultrasonic horn, and an ultrasonic power source to supply an electrical signal to actuate the transducer portion.

Abstract: A jaw member for use with a surgical instrument includes a support base, a jaw liner, and a jaw overmold. The support base has a proximal portion configured to be pivotably coupled to a surgical instrument, and a distal portion. The support base defines a channel that extends longitudinally between the proximal and distal portions and an aperture disposed in communication with the channel. The jaw liner includes an elongate body configured for receipt in the channel of the support base, and a projection extending from the elongate body and configured for receipt in the aperture of the support base. The jaw overmold overlaps at least a portion of the support base and the jaw liner to fix the jaw liner to the support base.

Abstract: A minimally invasive skin treatment system includes a platform having a recessed area on its bottom and one or more injection ports orthogonal to its top, each injection port including a through-hole to the recessed area. The system includes an injection device including a needle slidably disposed in a selective port such that the needle passes into the recessed area and percutaneously through a dermis disposed within the recessed area. A nozzle is configured to discharge a fluid at a high pressure in a direction orthogonal to an axis of the needle and parallel to the top of the platform to cut create a plane of dissection within the subcutaneous tissue.

Abstract: Polypectomy devices and methods for making and using polypectomy devices are disclosed. An example polypectomy device may include an elongate sheath having a proximal end region and a distal end region. A shaft may be slidably disposed within the sheath. A handle may be coupled to the proximal end region of the sheath. The handle may be designed to axially shift the shaft relative to the sheath. A snare may be coupled to the shaft. The snare may include a first region, a traction region, and a distal tip region. The first region may have a non-circular cross-sectional shape. The traction region may include a plurality of traction members. At a position between two adjacent traction members the snare may have a reduced cross-sectional area relative to the first region. The distal tip region may have a circular cross-sectional shape.

Abstract: A catheter for removing tissue from a body lumen include's a rotatable cutter. The cutter includes an annular cutting tip at the distal end portion of the cutter for removing tissue from the body lumen. An axial cavity is defined by an interior surface of the cutter and extends proximally from the annular cutting tip toward the proximal end portion of the cutter. An eccentric opening extends from the central cavity through the cutter to allow tissue removed from the body lumen by the annular cutting tip to pass proximally through the eccentric opening toward an interior passage of the catheter body. The offset opening is offset from the longitudinal axis of the cutter.

Abstract: An apparatus and method is disclosed for an intravascular balloon device having a balloon and a handle where a catheter tube extends between the two. The handle assembly includes an inflation device in fluid communication with the balloon. A medical tool is provided on the outer surface of the balloon for the treatment of intravascular conditions. The medical tool may be configured to score or remove atherosclerotic material.

Abstract: The present disclosure relates to the field of endovascular treatment. More particularly, the present invention uses a modified hydrogel intrasaccular occlusion device designed to implement an endovascular treatment to ameliorating or eliminating aneurysm recurrence, which hydrogel may optionally be impregnated with pharmaceutical compounds. The present invention also teaches the use of thin hydrogel coatings to ameliorate endovascular treatment related difficulties.

Abstract: Systems, apparatus, and methods are described for forming an incision in tissue for receiving a surgical instrument. A cutting device for forming the incision can be reversibly coupleable to an instrument, e.g., a dilator. The instrument may define a lumen configured to receive a wire that extends or is otherwise extendable through a puncture site. The cutting device can include a cutting element configured to be actuated to form the incision such that the incision extends form the puncture site and is sized to receive the instrument.

Abstract: The present invention generally relates to methods for preparing a skin graft without culturing or use of biologics.

Abstract: A trocar sleeve for minimally invasive surgery, having a first sleeve part, which has essentially the shape of a straight tubular piece with a longitudinal axis, and having a second sleeve part, which at least partly surrounds the first sleeve part in close contiguity and is movable during use with respect to the first sleeve part. The mobility of the second sleeve part in relation to the first sleeve part consists essentially only in rotatability of the second sleeve part around the first sleeve part, and in addition the first sleeve part and the second sleeve part each comprise on their distal axial ends a flange part that extends radially outward at an angle of less than 180 degrees from the respective sleeve part.

Abstract: In one embodiment the apparatus includes a first retractor, a second retractor, and a shaft. The shaft defines a central channel extending from a first end portion of the shaft to a second end portion of the shaft. The first retractor and the second retractor are configured to collectively form a lumen. The shaft is configured to be disposed within the lumen. In one embodiment method of disposing a graft within a body of a patient, includes making an incision in the body of the patient, inserting a medical device into the body of the patient through the incision, removing the shaft of the medical device from the body of the patient, and moving the first refractor within the body of the patient away from the second retractor.

Abstract: The disclosure provides, inter alia, methods of improving sperm function and related methods of fertilization, together with preparations of activated or potentiated sperm. The disclosure additionally provides articles of manufacture suitable for performing the methods provided by the invention. The methods provided by the disclosure, in some embodiments entail energy depletion with subsequent staged reintroduction of different energy sources.

Abstract: A dynamization device may comprise a sleeve, a shaft, a dial, a contact feature, and a biasing member. The shaft may comprise an interior section partially within an inner recess of the sleeve; a flat surface on the interior section of the shaft; and a plurality of external threads on the interior section of the shaft. The dial may comprise a body disposed partially within the inner recess; an annular lip; and internal threads secured to external threads of the shaft. The contact feature has an annular geometry disposed within the inner recess of the sleeve. The biasing member may be disposed around the interior section of the shaft, and disposed between the contact feature and a shoulder within the inner recess of the sleeve. Rotation of the annular lip may provide for compressive movement of the biasing member relative to the sleeve and shaft.

Abstract: The present invention includes an apparatus, kit and method for providing a bone fixation assembly for attachment to a bone to provide augmented support. The bone fixation assembly includes a screw having a screw head and a threaded shank. A first aperture is positioned about the screw head to receive a first longitudinal member and a first compression member that engages the first aperture to secure the first longitudinal member. The screw head has a second aperture positioned to receive a second longitudinal member and a second compression member that engages the second longitudinal member aperture to secure the second longitudinal member and provide augmented support.

Abstract: A surgical instrument comprises a first member defining a cavity and including a locking surface disposed with the cavity. The locking surface is engageable with a longitudinal member to fix a tether with the first member. A second member includes an inner surface that defines a longitudinal passageway configured for disposal of a surgical driver engageable with a spinal construct. The second member further includes at least one mating element being engageable with the spinal construct. An actuator is connected with the members and is configured to incrementally tension the tether. Systems, implants and methods are disclosed.

Abstract: A method of inserting a spinal stabilization system into a patient generally comprises inserting a first positioning tool through a first location on a patient's skin and along a path generally toward a first vertebral anchor, coupling an end of the first positioning tool to the first vertebral anchor, positioning at least a portion of a delivery device over a connecting element, and inserting the delivery device and the connecting element through the patient's skin at the first location and along at least a portion of the first positioning tool. The first positioning tool is configured to facilitate directing the delivery device and connecting element generally toward a second vertebral anchor within the patient's body.

Abstract: The present invention relates to an expansible intravertebral implant system comprising an intravertebral implant (1) with an expandable anterior part (11), which is expansible in a vertebral body, and a posterior part; and a pedicle fixation (2) having at least one hollow portion for receiving the posterior part. The present invention also relates to said expansible intravertebral implant system additionally comprising a posterior element (3), arranged partially outside the vertebra and rigidly connected to the pedicle fixation (2), for serving as an anchoring point for at least one intravertebral rod or at least one system of artificial ligaments.

Abstract: Orthopedic fixation devices and methods of installing the same. The orthopedic fixation device may include a coupling element and a bone fastener, whereby the bone fastener can be loaded into the coupling element through the bottom of a bore in the coupling element.

Abstract: A bone anchor having a rod housing including a base that has an internal groove oriented at an angle oblique to the longitudinal axis of the base, a capture ring situated within the groove and oriented at an angle oblique to the longitudinal axis, and a bone fastener extending into the rod housing and including a fastener head situated within the base and having a surface that mates with the capture surface of the capture ring to maintain a connection between the bone fastener and the rod housing.

Abstract: A spinal screw assembly is provided. The assembly may be provided with a screw and a movable head in which angulation of the screw relative to the movable head is constrained so that angulation within limits is allowed in one plane but lesser or no angulation is allowed in another plane. Methods to assemble the disclosed apparatus are also disclosed.

Abstract: Embodiments disclosed herein include systems for the treatment of spinal deformity in children by harnessing growth modulation without requiring vertebral fusion. In some embodiments, the system uses flexible or moveable elements to selectively apply and tune forces and moments to the spine instead of rigid fixation and vertebral segment fusion.

Abstract: A guiding apparatus for pedicle screws insertion, including: two orientation rods, used to be fixed on a bone to provide two non-parallel rod bodies; an orientation board, having a first orientation tube, a second orientation tube, a lengthy lateral opening, and a plurality of sleeve combinations, the second orientation tube having a vertical opening connected with the lengthy lateral opening, so that when one rod body of the two non-parallel rod bodies passes through the first orientation tube, the other rod body of the two non-parallel rod bodies will move through the lengthy lateral opening and enter the second orientation tube via the vertical opening; and a plurality of metal pins, used to be inserted into the bone through the plurality of sleeve combinations, and guide a plurality of pedicle screws to be screwed into the bone after inner sleeves of the sleeve combinations are removed.

Abstract: An embodiment includes a system comprising: a tulip including a slot to receive a linkage, first and second side walls that define a portion of the slot, and a ring that couples the first side wall to the second side wall; wherein the ring couples to the first side wall at a thinned first proximal fulcrum and to the second side wall at a thinned second proximal fulcrum and the ring pivots about the first and second proximal fulcrums when the ring is forced proximally; wherein the first side wall includes a first sidewall projection that projects past the first proximal fulcrum and the second side wall includes a second sidewall projection that projects past the second proximal fulcrum. Other embodiments are described herein.

Abstract: Apparatus and methods for bone fracture repair. The apparatus may include a structural support for positioning a first bone segment relative to a second bone segment. The apparatus may include an anchoring substrate. The anchoring substrate may be configured to compress the first bone segment to the second bone segment. The anchoring substrate may transmit tension from a distal bone segment anchor in the first bone segment to a proximal bone segment anchor in the second bone segment. The apparatus may be configured to be deployed percutaneously in an inner cavity of a bone. The apparatus may be installed in an open fracture. The apparatus may be expanded, self-expanding or configured for mechanically actuation. Some embodiments of the apparatus may include a central axis member that may be used in conjunction with expansion of one or both of the structural support and the anchoring substrate to configure the apparatus.

Abstract: An intramedullary device includes a central bridge region having a first end and a second end. The intramedullary device also includes a bone engaging feature at both the first end and the second end. At least one of the bone engaging features includes a first barb and a second barb which, in an unbiased condition, flare outwardly from a longitudinal axis of the central bridge region and which are capable of being elastically constrained to a constrained condition such that the first end of the central bridge region may be advanced into a hole in a first bone fragment when the first barb and second barb are elastically constrained. The first barb and second barb are prevented from being withdrawn from the hole in the first bone fragment when the first barb and the second barb are not constrained. The intramedullary device i) is cannulated, ii) generates a compressive load, and iii) comprises nitinol.

Abstract: Novel bone screw and plate assemblies including locking confirmation mechanisms are provided. In certain cases, a locking confirmation mechanism is operably attached to the plate, and comprises a toggling arm having an upper portion, a mid-portion and a lower portion. When a bone screw is positioned in a plate in an unlocked configuration, the locking confirmation mechanism assumes a first position. When the bone screw is positioned in the plate in a locked configuration, this causes the locking confirmation mechanism to pivot and assume a second position. The locking confirmation mechanism thus provides a convenient visual and/or tactile means to assess when the screw is in a locked configuration.

Abstract: A plate for fracture fixation, a system and methods are provided including a plurality of individually adjustable heads and various features and accessories to achieve: a.) superior fixation of the plate to osteoporotic diaphyseal bone; b.) improved visualization of the fracture line; c.) intraoperative adjustability to achieve better contact of the plate and the bone; d.) reduced risk of post-surgery tendon rupture; d.) improved fixation of small volar marginal fragments; e.) improved targeting and fixing of particular fractured bone fragments and, f.) reduced surgical operation time.

Abstract: The present disclosure provides a fastener that has a body that has an axis. The body comprises a head portion and at least one body portion projecting from the head portion. The at least one body portion has an actuating surface portion and is arranged such that at least a part of the at least one body portion is urged away from the axis when an actuating member is received along the axis and urges against the actuating surface portion. The at least one body portion has a substantially flat surface portion facing away from the axis.

Abstract: Stand alone fusion cage assemblies that can be secured to the adjacent vertebral bodies via an in-line approach that is substantially perpendicular to the anterior wall of the stand alone cage (or substantially parallel to the cage insertion direction).

Abstract: A bone implant and a manufacturing method thereof are provided. The bone implant is used for implanting a bone of a living body, such as bone, vertebra and alveolar bone. The bone implant includes an implanting body and a plurality of microstructures formed on a surface of the implanting body. An inner layer of the bone implanting body is made of metal including titanium or alloy including titanium, and an outer layer of the bone implanting body is titanium dioxide. Each microstructure has a height and a width, wherein the width is less than 2 micrometers and the height is less than 1 micrometer.

Abstract: A surgical instrument system and method of use is disclosed. The system includes a bone fixation pin and a surgical instrument configured for use with the bone fixation pin. The surgical instrument includes a sheath extending over the distal end of an elongated shaft and a locking mechanism operable to permit selectively movement of the elongated shaft along the longitudinal axis relative to the sheath.

Abstract: A method for the selective elevation and separation of tissues comprised of multiple layers and a surgical instrument for performing the method. The method may be performed without the requirement of a solid mechanical device insertion or transection through the mucosal layer. In particular, the method and surgical instrument may be used for the selected separation and/or resection of selected portions of benign or malignant tissues (e.g. defining tissue planes, polyp elevation and removal, submucosal tissue tunnelling, endoscopic mucosa resection, etc).

Abstract: A treatment-energy applying structure includes a flexible substrate having a wiring pattern having a heat-generation region and a connection region. A heat transfer plate faces a surface of the flexible substrate, and transfers heat to a body tissue. An adhesive sheet, having heat conductivity, is disposed between the flexible substrate and the heat transfer plate to cover the entirety of the heat-generation region and the heat transfer plate. A region of the adhesive sheet protrudes from the heat transfer plate to cover a region of the connection region. A pair of lead wires connects to the connection region outside of the covered region. The adhesive sheet is longer than the heat transfer plate and shorter than the flexible substrate. A gap between an end of the heat transfer plate and the lead wires is longer than a diameter of the lead wires or a thickness of the heat transfer plate.

Abstract: A treatment energy application structure includes a flexible substrate having an electric resistance pattern and a lead wire connection portion. A heat transfer plate faces the flexible substrate and transfers heat to the body tissue. An insulating adhesive sheet is interposed between the flexible substrate and the heat transfer plate. The insulating adhesive sheet comprises a first area to cover an entire surface of the electric resistance pattern and the heat transfer plate and a second area protruding from the heat transfer plate to cover a part of the lead wire connection portion. The heat transfer plate has a chamfered corner facing the insulating adhesive sheet. An adhesive may adhere the second area to at least one of the heat transfer plate and the substrate. The insulating adhesive sheet may adhere the substrate to both the heat transfer plate and the bridge portion of a cover.

Abstract: An electrosurgical generator includes a gain-compensated full bridge topology. Gain nonlinearity is corrected by applying impedance and phase correction factors to a control loop to achieve a linear gain structure. In embodiments, gain compensation is performed by comparing an RF setpoint signal with a calculated output signal to generate a first error signal. An impedance correction factor is applied to the first error signal to generate a second error signal. The second error signal is processed by a proportional-integral-derivative controller to generate a phase control signal. A phase control correction factor is applied to the phase control signal to generate a corrected pulse width modulation driving signal, which is used to generate PWM driving signals for a full-bridge inverter. One or more sensors provide feedback for comparison with the RF setpoint.

Abstract: An electrosurgical system includes an electrosurgical probe connected to a control console, wherein the probe is capable of coagulating and ablating tissue depending on a selected operating mode. Before operating the system, probe-specific data stored in a memory device associated with the probe is read by a processing device in the console. The data includes source impedance values specific to a coagulation or cutting mode of operation. A constant duty cycle value for a modulated cutting mode also is provided. Depending on the operating mode selected, an RF generator adjusted to have a predetermined source impedance value provides a voltage value to the probe. During the duty-cycled mode, the RF generator generates an instantaneous voltage value output for a duty cycle portion that is less than 100% of a time period, which value is no less than a maximum continuous average voltage value for the electrosurgical probe.

Abstract: A controller for an electrosurgical device and related methods and devices are disclosed. The controller has a processing component to: (a) derive a power factor of power applied to the electrosurgical device; and (b) responsive to the deriving a power factor, assign a circuit status to a circuit comprising the electrosurgical device. IF (PF?0) and ((Vrms/Irms)?T), THEN the circuit status is “open”. IF (PF?0) and ((Vrms/Irms)<T), THEN the circuit status is “short”. PF is the power factor. Vrms is the root mean square of a voltage associated with the power applied to the at electrosurgical device. Irms is the root mean square of a current associated with the power applied to the electrosurgical device. T is a threshold value.

Abstract: Electrosurgical lysing devices and related systems and methods. In some embodiments, the lysing device may comprise a lysing tip comprising a plurality of beads and at least one lysing member, such as a lysing rod, defining at least one lysing segment extending between each pair of adjacent beads. The at least one lysing member may extend through a tunnel extending at least partially through each of the plurality of beads so as to define the at least one lysing segment between each pair of adjacent beads.

Abstract: A system includes an energy source and a surgical device. The energy source has a receptacle configured to delivery energy to the surgical device through a receptacle. The surgical device is configured to deliver the energy to tissue. The surgical device includes a plug selectively engagable to the receptacle to couple the surgical device to the energy source. The plug includes a prong configured to mechanically transition from a condition permitting engagement of the plug and the receptacle to another condition inhibiting engagement of the plug with the receptacle upon reaching a predetermined usage threshold.

Abstract: An end effector for an electrosurgical instrument includes a pair of opposing first and second jaw members movable between an open position in which the jaw members are disposed in a spaced relation relative to one another, and a closed position in which the jaw members cooperate to grasp tissue therebetween. A first sealing electrode is located on the first jaw member, and a second sealing electrode is located on the second jaw member. One or more stop members are disposed on the sealing electrodes, the one or more stop members being formed of a compliant material such that they are capable of deforming when the jaw members are moved to their closed position with tissue grasped therebetween.

Abstract: A tissue resection device comprises inner and outer coaxial sleeves. The outer sleeve has a cutting window formed therein, and the inner sleeve has a distal cutting end that can be reciprocated past the cutting window. The sleeves comprise electrodes to provide electrosurgical cutting, and an edge portion of the window includes a dielectric material.

Abstract: Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a catheter for use in cardiac mapping and/or ablation. The catheter may include an elongate catheter shaft having a distal ablation electrode region capable of ablating tissue. An electrode assembly may be coupled to the distal ablation electrode region. The electrode assembly may include a flexible circuit having one or more electrodes disposed thereon.

Abstract: The present invention relates to comprehensive systems, devices and methods for delivering energy to tissue for a wide variety of applications, including medical procedures (e.g., tissue ablation, resection, cautery, vascular thrombosis, treatment of cardiac arrhythmias and dysrhythmias, electrosurgery, tissue harvest, etc.). In certain embodiments, systems, devices, and methods are provided for delivering energy to difficult to access tissue regions (e.g. peripheral lung tissues), and/or reducing the amount of undesired heat given off during energy delivery.

Abstract: A medical laser system includes a crystal-based laser, an electrosurgery or electrocautery device, a power supply for powering the crystal-based laser and the electrosurgery or electrocautery device, and a controller operably connected to the crystal-based laser, the electrosurgery or electrocautery device, and the power supply. The controller is programmed to: (a) activate the crystal-based laser by controlling power supplied by the power supply to the laser responsive to a laser activation input by a user; and (b) activate the electrosurgery or electrocautery device by controlling power supplied by the power supply to the electrosurgery or electrocautery device responsive to an electrosurgery or electrocautery device activation input by the user.

Abstract: A method of operating a flashlamp in a skin treatment system comprises the steps of charging capacitor, discharging the capacitor through a flashlamp, and interrupting the discharge of the capacitor through the flashlamp at a predetermined time based on at least one condition caused by the discharge of the capacitor through the flashlamp.

Abstract: This invention relates to an advance in the delivery of laser beams to internal surgical sites using optical fibers with a novel distal tip design made using a fusion assembly procedure suitable for directing laser beams out of the side of an optical fiber. This side-fire fiber delivery tip assembly is fabricated by fusing a transparent tube onto the distal ends of a laser beam delivery fiber and an associated coaxial stub fiber that have beveled and parallel end faces that meet inside of the transparent tube. The result is a rugged fiber delivery tip assembly that is almost entirely solid, except for a very narrow gap between the beveled end surfaces of the two fibers. A loose fitting transparent capsule is placed over this fiber tip to contain a transparent perfluorocarbon lubricating oil or a perfluorocarbon heat-transfer agent that serves as a cooling agent for the fiber tip assembly.

Abstract: Methods and devices for improving the interface between a surgeon and an operating medical assistant or between the surgeon and an endoscope system for laparoscopic surgery. A device is useful for controlling an endoscope system for laparoscopic surgery and includes a wearable interface for enhancing the control of an endoscope system during laparoscopic surgery.

Abstract: Disclosed herein are a computer assistance method for the reduction of a fracture and a computing system for assisting the reduction of a fracture. The computer assistance method includes: generating a first model of a first bone, which is a treatment target, based on a pre-operative medical image; generating a second model, assumed to be obtained after the restoration of the first bone, based on the pre-operative medical image; acquiring a third model in which the spatial information of the first model has been updated by incorporating, into the spatial information, the movement of the first bone occurring during treatment after the installation of markers onto the first bone; and generating overlay visual information based on the second and third models registered onto the same space.

Abstract: A method of generating a correction plan for correcting a deformed bone includes inputting to a computer system a first image of the deformed bone in a first plane and inputting to the computer system a second image of the deformed bone in a second plane. Image processing techniques are employed to identify a plurality of anatomical landmarks of the deformed bone in the first image. The first image of the deformed bone is displayed on a display device. A graphical of the deformed bone is autonomously generated and graphically overlaid on the first image of the deformed bone on the display device, the graphical template including a plurality of lines, each line connected at each end to a landmark point corresponding to one of the anatomical landmarks. A model of the deformed bone may be autonomously generated based on the graphical template.