Abstract: In accordance with aspects of the present invention, an instrument is provided. An instrument seal according to some embodiments includes a seal body that can be captured between an upper part and a lower part of an instrument guide; and openings in the seal body that align with channels on the instrument guide, wherein the seal body seals against doors in the lower part and an instrument shaft inserted through the openings.

Abstract: A device for use with a uterine tamponade apparatus, such as the Bakri® postpartum hemorrhage balloon, is disclosed. The device comprises an anchor for deployment within the vagina to securely retain the balloon in its proper position within the uterine cavity, allowing the balloon to function as intended for the control and management of postpartum hemorrhage and uterine bleeding. Methods of use of the vaginal anchor are also disclosed.

Abstract: Components, systems and kits for capturing and removing tissue from mammalian bodies include a tissue container that may be introduced into a body cavity and within which a tissue specimen may be placed, cut and removed from the body cavity. Methods of using these components, systems and kits are also described.

Abstract: Implementations described herein include a system that may include a deliver device, an annular anchor and an implant. The delivery device may include a distal end, a proximal and a lumen extending from the distal end to the proximal end. The annular anchor may be removably coupleable to the distal end of the delivery device. The annular anchor may be implantable at a target site in a patient via manipulation of the delivery device. The delivery device may be extendable outside the patient when the anchor is implanted at the target site. The implant may be deliverable through the delivery device to the target delivery site and implantable through the annular anchor. The delivery device may be coupled to the annular anchor to control a trajectory of the implant to the target site.

Abstract: A spinal alignment system can include a rod and a plurality of uniplanar screw assemblies that include a screw, a cap, and a housing. The screw and cap can be configured such that the relative angular displacement between the screw and the cap is limited to a first limit angle in a first plane and to a second limit angle in a second plane that is perpendicular to the first plane, the second limit angle being larger than the first limit angle. The housing can be coupled to the cap and configured to maintain the cap in proximity with the head of the screw. The housing can have two elongated elements forming a U-shaped saddle. The alignment system can also include a plurality of locking cap assemblies that capture the rod within the U-shaped saddle and are tightened to fixedly couple the rod to the respective uniplanar screw assemblies.

Abstract: A spinal fixation device is provided. The spinal fixation device includes a body portion including a stud portion defining a first annular groove. An outer housing is positionable on the stud portion of the body portion. An inner housing defines a second annular groove and is positionable between the outer housing and the stud portion. A ring member is positionable within each of the first and second annular grooves of the respective stud portion and inner housing to lock the inner housing to the body portion and to fixedly couple the outer housing to the stud portion.

Abstract: A receiver for engaging a bone stabilizing element includes a receiver portion connectable to the stabilizing element, and a base portion connectable to a bone of a patient. The base portion may connect to the bone with a bone screw, for example a polyaxial bone screw, and the receiver portion may connect to the stabilizing element, for example a rod, using a set screw. The receiver portion and the base portion are slideably connected to each other, coupled and constrained in relative movement, by overlapping portions. Axial rotation between the receiver portion and the base portion is enabled by changing the relative dimensions of overlapped portions.

Abstract: The present disclosure includes a polyaxial bone fixation element for use in spinal fixation to interconnect a longitudinal spinal rod with a patient's vertebra. The polyaxial bone fixation element preferably includes a bone anchor, a collet, a body, and a locking cap. The polyaxial bone fixation element preferably enables in-situ assembly. That is, the polyaxial bone fixation element is preferably configured so that in use, the bone anchor may be secured to the patient's vertebra prior to being received within the body. Accordingly, the polyaxial bone fixation element enables a surgeon to implant the bone anchor without the body to maximize visibility and access around the anchoring site. Once the bone anchor has been secured to the patient's vertebra, the body can be snapped-onto the bone anchor. The bone anchor preferably also includes a second tool interface so that a surgical instrument can be directly coupled to the bone anchor.

Abstract: An orthopedic connection assembly is described that comprises a housing member for receiving an implant that is operably connected to a receiving member for receiving an anchor member. The connection assembly is configured to have a locking mechanism that secures and fixes the relative orientation between the implant and the anchor member. The connection assembly can comprise a plate member receivable within the housing member. When a securing member such as a set screw is introduced downwardly into the housing member to secure the implant, the securing member applies a lateral force to the plate member, which presses against an interference member within the receiving member. The interference member presses against the anchor member, such that the anchor member is fixed in a position relative to the implant.

Abstract: An implant for the stabilization of bones or vertebrae is provided, the implant being a solid body including a longitudinal axis that defines a longitudinal direction and including a flexible section that has a surface and has a length in the longitudinal direction, the flexible section including at least one cavity located near the surface and having a width in the longitudinal direction that is smaller than the length of the flexible section, the at least one cavity being connected to the surface through at least one slit, and a width of the slit in the longitudinal direction being smaller than the width of the cavity.

Abstract: A surgical system includes an implant having a first attachment mechanism and an insertion instrument having a proximal end, a distal end, and a second attachment mechanism disposed at the distal end for removable connection with the first attachment mechanism. The proximal end of the insertion instrument is pivotable with respect to the implant. The insertion instrument can include an inserter and a guide. A method of using the surgical system is provided.

Abstract: The invention relates to an extension device (2) for a bone anchor (4), in particular for a pedicle screw having an axial longitudinal direction (16), a circumferential direction (18) concentric thereto and a radial direction (20), wherein the extension device (2) is extended in the axial longitudinal direction (16) and can be detachably fixed to the head (8) of the bone anchor (4), wherein the extension device (2) comprises two shell parts (22) that are separate from each other and extended in the longitudinal direction 16, characterized in that, the extension device further comprises a sleeve-like housing part (60) that can be slid in the axial longitudinal direction (16) onto the two shell parts (22) which are separated from each other and detachably fixed to the head of the bone anchor and, in the applied state, limits and defines a tunnel-like access (106) to the bone anchor (4) that extends in the axial direction (16).

Abstract: Implementations described herein may include a system for manipulating implants coupled by a cord. The system may include a tensioner and a counter tensioner. The tensioner may include a nose assembly and a cord lock assembly for applying tension to the cord. The nose assembly may include a piston having a lumen extending therethrough for receiving the cord and a spring positionable in contact with an indicator region of the piston. The counter may be releasably coupleable to a head of an implant at a proximal end thereof and may guide the cord to a port proximate the distal end thereof, the port for receiving the nose assembly. The counter tensioner may enable translation of the implant relative to another implant implanted in an adjacent or nearby vertebrae. The indicator region of the piston may be visible through a window in a tensioner main body and may indicate cord tension when the nose assembly of the tensioner is coupled to the port of the counter tensioner and engaged with the cord.

Abstract: A system, a method, and instruments for manipulating a surgical cord into spinal implants to assist in correcting a spinal deformity are described. The system may include a tensioner, a tensioner extension, and a counter tensioner. One of the instruments can include an elongate body, a dual coupler, and a nose member. The elongate body has a flexible cylindrical member adapted to carry tension along a longitudinal axis, where the flexible cylindrical member is sized to receive a surgical cord through a lumen within the flexible cylindrical member. The dual coupler is disposed on a proximal end of the elongate body, and include a bore for receiving a nose portion of a tensioner and for guiding the surgical cord into the tensioner. The nose member is disposed on a distal end of the elongate body, and be adapted to discharge the surgical cord from the elongate body.

Abstract: A two-part hammertoe system includes a double-sided hammertoe implant and a window capsule. The double-sided hammertoe implant includes a first end configured to couple the first end to a first bone and a second end comprising a plurality of expandable tines having a predetermined arrangement. The plurality of expandable tines are expandable from a first position having a first diameter to a second position having a second diameter. The second diameter is greater than the first diameter. The window capsule includes a closed distal end, a side wall extending proximally from the closed distal end, and a wedge extending from the distal end into an inner volume defined by the closed distal end and the side wall. The window capsule is sized and configured to couple to a second bone. The wedge is sized and configured to transition the plurality of tines from the first position to the second position.

Abstract: A fastener, for example a bone screw, is sized to pass through a hole of an implant, for example a bone plate, the fastener having a shaft or anchor portion engageable with body tissue, and a head portion. A locking cap secures to the bone plate and covers the head to block the head and inhibit screw back out. Alternatively, or additionally, a locking disc located in the plate hole resiliently deflects downward to allow screw insertion, but is blocked to limit or prevent upward deflection so that screw back out is inhibited.

Abstract: An orthopedic plate and fastener system is provided for fixation of bones which has an implant that can selectably be used to achieve fixed angle and variable locking of the fasteners, as well as non-locking of the fasteners. The system includes a variable locking assembly that includes a locking insert, having threads which mates with internal threads of a through opening in the implant. The system also provides for locking fixed angle fixation, and non-locking variable angle fixation, all of which can be used with the threaded holes of the plates. The locking insert is provided on a ring driver, which is similar to or acts as the drill guide used with the locking fasteners of the present. Thus, the invention also relates to a method of enabling surgery where the surgeon can select the mode of fixation of fasteners between variable axis locking, variable axis non-locking, and fixed angle locking fixation, all utilizing the same fastener opening within the implant.

Abstract: An interbody spinal fusion implant includes a body and a faceplate secured to the body. A recess is formed on a front face of the faceplate and is at least partially bounded by an interior surface. A first screw hole and a spaced apart first locking hole pass through the faceplate from interior surface of the recess. A first locking screw has a shaft threaded into the first locking hole. The first locking screw blocks removal of a bone screw from within the first screw hole when the locking screw is in a retracted position.

Abstract: Various embodiments provide an apparatus for treating pectus excavatum. A pectus bar apparatus includes at least one elongated bar having an offset bend between a first end and a second end, at least one aperture near the first end and at least one aperture near the second end, a planar stabilizer extending orthogonally from the elongated bar, and a pair of opposing rib reveals located between the first end and the planar stabilizer. A pectus excavatum treatment kit and a method for utilizing that kit are also provided.

Abstract: In the event of bone fractures, in particular comminuted fractures, having multiple bone fracture pieces, a quick and safe operation can be possible when implements (1) are used for stabilizing the affected bone (6). The main body (2) of these implements is an angle profile (15), wherein long recesses (17-19) are provided in the plate side pieces (10, 11). This facilitates any bending that may become necessary about the longitudinal axis (9) and the transverse axis (16). In this way, it is possible to achieve a high level of stability for the operated region, in order to guarantee an early functional exercising of the neighboring joints without risking the bone fragments shifting again.

Abstract: An adjustable balloon that includes a handle having an inflation port, an access cannula, a rotary handle, an inner sleeve and sharp tip. The inner sleeve extends within the access cannula to support compliant, inflatable structure. The access cannula may be retracted into the handle by operation of the rotary handle to expose the inflatable structure, such that the inflatable structure may have an adjustable length. The access cannula may include length indicators to show a length of the inflatable structure as a result of the access cannula being withdrawn into the handle.

Abstract: Driver instruments are disclosed herein with various features for improving usability, easing the task of cleaning or sterilizing the instrument, reducing patient trauma associated with use of the instrument, and/or reducing the cost and assembly burden of the instrument. For example, a driver instrument can include a guide sleeve to protect patient tissue from damage caused by rotating components of the instrument or a bone anchor assembly coupled thereto, and to protect extension tabs of the bone anchor assembly from inadvertent separation. By way of further example, an instrument can include a preload assembly for maintaining engagement of a driver shaft of the instrument with a bone anchor assembly. As yet another example, an instrument can consist of a small number of components which are configured for simple, tool-free assembly and disassembly. An instrument can also be configured for use with bone anchor assemblies with and without extension tabs.

Abstract: A surgical impact tool comprises an electromagnetic impactor hermetically sealed within a sterilizable housing having one or more external mechanical coupling for transmitting an impact to an object external to the tool. The housing also contains an energy storage medium rechargeable through the hermetic seal, and electronic controls operable through the hermetic seal.

Abstract: According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery.

Abstract: An ablation assembly includes a handle, a catheter assembly and a connector locking assembly. The catheter assembly includes: a catheter shaft, a balloon and a connector at the distal and proximal ends of the catheter shaft, and a delivery tube extending between there between. The connector includes a connector body secured to the proximal end and a plug secured to the delivery tube, the plug and delivery tube movable axially and rotationally. The handle includes an open portion receiving the plug and the connector body. The connector locking assembly includes: means for simultaneously automatically connecting the plug and the connector body to the handle to place the connector in a load state prior to use, and means for automatically releasing the connector body and thereafter the plug from the handle to place the connector in an eject state to permit the connector to be removed from the handle.

Abstract: A tumor ablation system includes a heating needle and a power supply device. The heating needle includes a rigid tubular shell. The heating needle further includes a heating element and a non-heating element; the heating element has at least one heating wire, a central cylindrical object and a distal part of the shell. The heating wire and the central cylindrical object are inside the shell. The heating wire is electrically coupled to the non-heating element, and coiled on the central cylindrical object. The distal part of the shell covers the coil formed by the heating wire on the central cylindrical object. When the heating wire is charged with electricity the heating wire generates thermal energy that is conducted to the distal part of the shell. The power supply device couples to the non-heating element, and provides electricity to the heating needle.

Abstract: Various exemplary methods, systems, and devices for controlling electrosurgical tools are provided.

Abstract: Surgical systems and methods are provided for controlling actuation and movement of various surgical devices.

Abstract: Surgical systems and methods are provided for controlling actuation and movement of various surgical devices.

Abstract: An electrosurgical system includes an electrosurgical instrument and an electrosurgical generator. The generator includes an energy source having an active terminal and a return terminal that outputs electrosurgical energy and a controller that controls the energy source. A cable is coupled between the electrosurgical instrument and the electrosurgical generator where the cable includes a first conductor and a second conductor. The controller is configured to electrically couple the active terminal and/or the return terminal to the electrosurgical instrument using the first conductor and/or the second conductor based on whether the electrosurgical instrument is a monopolar instrument or a bipolar instrument.

Abstract: An electrosurgical energy delivery apparatus includes an energy delivery circuit, a control circuit and an energy-harvesting system with a plurality of energy-harvesting circuits and a voltage regulator that provides a regulated DC voltage to the energy delivery circuit and/or the control circuit. The energy delivery circuit receives an electrosurgical energy signal having a primary frequency and selectively provides the electrosurgical energy signal to an energy delivery element. The control circuit connects to the energy delivery circuit and selectively enables the flow of electrosurgical energy to the energy delivery element. The plurality of energy-harvesting circuits each include an energy-harvesting antenna tuned to a particular frequency, a matched circuit configured to receive an RF signal from the energy-harvesting antenna, rectify the RF signal and generate a DC signal, and an energy storage device that connects to the voltage regulator to receive and store the DC signal.

Abstract: The invention relates to a medical probe signal generator. More particularly, it relates to a medical probe signal generator architecture. The present invention further relates to a system including a medical probe signal generator having an automatic probe type detector for detecting an identifier and at least one instrument cable comprising the identifier.

Abstract: An ablation device of a non-invasive radio-frequency ablation system includes a substrate having a first surface; a first electrode disposed on the first surface; a second electrode disposed on the first surface and adjacent to the first electrode; a moving unit electrically connected to the second electrode for moving the second electrode to regulate the distance between the second electrode and the first electrode; and a radio frequency generator connected to the ablation device for providing a radio frequency current to the first electrode and the second electrode. According to a method using the ablation device, the first and second electrodes are brought into contact with a third surface belonging to a subject in need of treatment, and the radio frequency current is applied to the electrodes to carry out a treatment procedure. The treatment depth and area are adjusted by changing the relative distance between the electrodes.

Abstract: A surgical system includes an electrosurgical tool configured to be releasably coupled to a surgical robotic system having a control system. The tool has a shaft having an end effector with treatment electrodes configured to apply electrosurgical power to a tissue, and aspiration and irrigation tubes having ports in the vicinity of the electrodes. The control system can control a flow rate of an irrigation fluid based on deviation of power delivered by the electrodes to the tissue from a power set point, or based on an aspiration rate that is controlled based on tissue impedance. The tool can have first and second ports and a conduit configured to selectively provide or aspirate fluids through at least one of the ports. At least one of a flow rate and an aspiration rate are controlled by the control system based on a rotational angle of the shaft relative to a ground.

Abstract: A surgical system includes an electrosurgical tool configured to be releasably coupled to a surgical robotic system having a control system. The tool has a shaft having an end effector with treatment electrodes configured to apply electrosurgical power to a tissue, and aspiration and irrigation tubes having ports in the vicinity of the electrodes. The control system can control a flow rate of an irrigation fluid based on deviation of power delivered by the electrodes to the tissue from a power set point, or based on an aspiration rate that is controlled based on tissue impedance. The tool can have first and second ports and a conduit configured to selectively provide or aspirate fluids through at least one of the ports. At least one of a flow rate and an aspiration rate are controlled by the control system based on a rotational angle of the shaft relative to a ground.

Abstract: An ablation device of a non-invasive radio-frequency ablation system includes a substrate having a first surface; a first electrode disposed on the first surface; a second electrode disposed on the first surface and adjacent to the first electrode; a moving unit electrically connected to the second electrode for moving the second electrode to regulate the distance between the second electrode and the first electrode; and a radio frequency generator connected to the ablation device for providing a radio frequency current to the first electrode and the second electrode. According to a method using the ablation device, the first and second electrodes are brought into contact with a third surface belonging to a subject in need of treatment, and the radio frequency current is applied to the electrodes to carry out a treatment procedure. The treatment depth and area are adjusted by changing the relative distance between the electrodes.

Abstract: An electrosurgical system includes an electrosurgical unit electrically coupled to a surgical retractor. The electrosurgical unit includes an RF output and an RF return. The surgical retractor includes a return pad electrically coupled to the RF return of the electrosurgical unit. The electrosurgical unit includes an RF output configured to be coupled to an electrosurgical device, such as an electrosurgical device configured in a monopolar mode. A controller is configured to determine an impedance in tissue at a surgical area electrically disposed between the RF output and the and the RF return. The surgical retractor includes a handle and a blade configured to interface with tissue. The blade includes a return electrode.

Abstract: A resecting probe includes a shaft assembly having an outer sleeve and an inner sleeve. The outer sleeve has an axial bore and an outer window in a distal side thereof, and the inner sleeve has an axial extraction channel and inner window in a distal side thereof. The inner sleeve is rotationally disposed in the axial bore of the outer sleeve to allow the inner sleeve window to be rotated in and out of alignment with the outer sleeve window, and the shaft assembly forms a flow aperture in a distal portion when the inner cutting window and the outer cutting window are out of alignment. An electrode is carried on the inner sleeve, and a motor drive is coupled to rotate the inner sleeve relative to the outer sleeve.

Abstract: An apparatus includes a body, a shaft assembly, an end effector, and an articulation section. The articulation section is longitudinally interposed between a distal end of the shaft assembly and a proximal end of the end effector. The articulation section is configured to flex to thereby provide deflection of the end effector away from the longitudinal axis of the shaft assembly. The articulation section includes a first frame member, a second frame member, and a sleeve. The proximal end of the second frame member is proximal to the proximal end of the first frame member. The sleeve is disposed about the first and second frame members.

Abstract: Various exemplary methods, systems, and devices for controlling electrosurgical tools are provided.

Abstract: Various exemplary methods, systems, and devices for controlling electrosurgical tools are provided.

Abstract: Various exemplary methods, systems, and devices for controlling electrosurgical tools are provided.

Abstract: An apparatus includes a shaft assembly and an end effector. The shaft assembly includes an outer sheath, at least one irrigation conduit, and at least one suction conduit. The end effector includes a first electrode, a second electrode, and a web. The electrodes extend distally relative to a distal end of the outer sheath. The electrodes are operable to apply bipolar RF energy to tissue. The web extends laterally between the first and second electrodes. The web is positioned distal to the distal end of the outer sheath.

Abstract: A surgical instrument including a housing, an actuator operably associated with the housing, a shaft extending from the housing, an end effector assembly disposed at an end portion of the shaft, and a drive assembly operably coupling the actuator and the end effector assembly with one another such that actuation of the actuator manipulates the end effector assembly. The drive assembly includes a proximal sleeve defining a longitudinal axis and an interior lumen extending longitudinally therethrough, a drive bar including a proximal portion and a distal portion, and a lock washer configured to engage the proximal portion of the drive bar with the proximal sleeve such that the proximal portion of the drive bar is disposed within the interior lumen of the proximal sleeve and positioned offset relative to the longitudinal axis of the proximal sleeve. Methods of assembling such drive assemblies are also provided.

Abstract: In a treatment system, an energy treatment instrument includes a pair of grasping pieces. An energy output source outputs electric energy to the energy treatment instrument, thereby applying treatment energy to a blood vessel grasped between the grasping pieces. A measurement section measures a blood pressure at a site related to the grasped blood vessel. A processor controls output of the electric energy from the energy output source based on a measurement result obtained by the measurement section, and thereby switches an actuation state of the energy treatment instrument between a first mode for coagulating the blood vessel and a second mode for coagulating the blood vessel target that is different from the first mode.

Abstract: Surgical systems and methods are provided for controlling actuation and movement of various surgical devices.

Abstract: Disclosed herein are a skin treatment apparatus using RF energy and a skin treatment method using the same. There are provided a skin treatment apparatus using RF energy, including a first handpiece configured to include a first electrode unit coming into contact with a skin surface and to form perforations through which an agent penetrates by transferring RF energy to the skin surface through the first electrode unit, a second handpiece configured to include a second electrode unit inserted into the inside of the skin and to insert the second electrode unit into the inside of the skin into which the agent has penetrated and transfer the RF energy, and a controller configured to control parameters of the RF energy transferred to the first electrode unit and the second electrode unit, and a treatment method using the same.

Abstract: A medical instrument includes a shaft, multiple electrodes and a vibration generator. The shaft is configured for insertion into a body of a patient. The multiple electrodes are fitted at a distal end of the shaft and are configured to deliver Radio Frequency (RF) energy for ablation at multiple respective locations in tissue. The vibration generator is configured to vibrate the multiple electrodes for providing cooling to the tissue in a vicinity of the locations.

Abstract: The present disclosure relates to a stent delivery system. According to the present disclosure, it is possible to minimize the current flow distance in the in-body by integrally conducting two poles to the electrocautery tip, thus enhancing the treatment stability.

Abstract: In one aspect, devices for light treatment of skin are described herein. A device described herein, in some embodiments, comprises an interior compartment having a proximal end and a distal end, and an optical aperture disposed at the distal end. The device also comprises a laser or BBL source that produces a laser or BBL beam. The laser or BBL beam has a first optical path within the interior compartment, between the proximal end and the distal end. Additionally, the first optical path exits the interior compartment through the optical aperture. The device further comprises an imaging system that receives a return signal from the aperture. The return signal received from the aperture has a second path within the interior compartment. Further, a selectively reflective optical element is disposed in the first and second optical paths. The selectively reflective optical element generally transmits the laser or BBL beam.