Abstract: This invention pertains to the field of medical diagnostics which is used to take a sample of blood vessel, called BLOOD VESSEL SAMPLE, for investigation purposes. The blood vessel sample kit composed of flexible clips attached with the stand, having tooth on the lower surface on either side of the clips. The blood vessel sample kit also having a triple scissors with a spring handle and three sets of upper and lower blades, purposed to cut off a small portion of the blood vessel, to make the vascular endothelium exposed, easy for culturing. The blood vessel sample is taken from the VISIBLE VASCULAR WEB of the SUPRA TENON VASCULAR WEB. The purpose of the blood vessel sample taking is to study the VASCULAR ENDOTHELIAL RESPONSE TO DIABETES—VERD, which is a part of conjunctival vasculopathy.

Abstract: An assembly including a bougie and a sheath for use in performing a gastroplasty for dividing a stomach of a patient into a sleeve receiving food and a bypass portion. The bougie includes an elongated body having a segment being shaped to follow a lesser curve of the stomach, and an extension member being movable within the stomach for positioning a distal portion thereof away from a gastroesophageal junction of the stomach and to define a fluid passage between the sleeve and the bypass portion. The sheath has an elongated main lumen in which the bougie is inserted and the sheath is translatable along the bougie to selectively expose the extension member of the bougie to perform its guiding action, or hide the extension member to ensure secure displacement of the bougie within the stomach and along the oesophagus.

Abstract: An endovascular device for providing at least partial occlusion in a blood vessel in a subject, e.g. for improving Cardiopulmonary Resuscitation. The device comprises a balloon catheter to be inserted in a blood vessel for inflation therein. To increase the flexibility and safety in use of the device and to enable use under controlled and less controlled environments, the device comprises a first interfacing means configured to connect to a first manually operated inflation means and being in fluid communication with a junction; a second interfacing means configured to connect to a second power controlled inflation means and also being in fluid communication with the junction, and an electronic control unit configured to receive the occlusion parameter from the sensor and to provide an instruction set for manually operated inflation or for automatically operated inflation based on the occlusion parameter.

Abstract: Disclosed herein is a bowl-shaped neck bridge with a distal-facing concavity and a central lumen. The neck bridge is inserted and expanded within a cerebral aneurysm. The, embolic members (such as embolic coils, embolic ribbons, or string-of-pearls embolic strands) are inserted through the central lumen into the aneurysm sac.

Abstract: A system for treating an aneurysm comprises an elongate flexible shaft and an expandable member. An expandable scaffold is disposed over the expandable member and may be expanded from a collapsed configuration to an expanded configuration. A double-walled filling structure is disposed over the scaffold and has an outer wall and an inner wall. The filling structure is adapted to be filled with a hardenable fluid filing medium so that the outer wall conforms to an inside surface of the aneurysm and the inner wall forms a substantially tubular lumen to provide a path for blood flow. In the expanded configuration the scaffold engages the inner wall of the filling structure. A tether is releasably coupled with the filling structure and the flexible shaft thereby constraining axial movement of the structures relative to each other.

Abstract: An anti-hemorrhage device, and an anti-hemorrhage kit, includes a rigid platform and a compression device adjustably secured to the rigid platform. The kit also includes a gastroesophageal aortic occlusion device.

Abstract: This disclosure relates to assemblies and methods for repairing bone defects. The assemblies disclosed herein may be utilized for determining a dimension of a surgical site and removing bone prior to positioning a graft and/or implant at the surgical site.

Abstract: A surgical instrument includes a first member defining an axis and having a scraping surface configured to scrape tissue. A second member includes a cutting surface that is rotatable relative to the first member. The second member has a maximum length defined by opposite end surfaces of the second member. The end surfaces are each disposed within the first member. A third member includes an outer surface defining at least a portion of a passageway configured for disposal of the scraped tissue. The third member is fixed with the first member. The cutting surface is rotatable relative to the third member to transfer the scraped tissue along the axis. Systems and methods are disclosed.

Abstract: A piezoelectric device comprising: (a) a handpiece for holding by a user; (b) a cutting insert for said handpiece; (c) an ultrasound transducer disposed within the handpiece, the ultrasound transducer capable of providing first and second ultrasound frequency vibrations to the cutting insert in response to an electrical signal; and (d) a switch allowing the user to control the electrical signal and thereby provide either said first or second ultrasound frequency vibrations to the cutting insert. The device is useful in a method of placing an implant into an implant site comprising cutting overlying gingival tissue at a first ultrasound frequency capable of cutting soft tissue, then switching to a second ultrasound frequency capable of cutting the underlying jawbone.

Abstract: A surgical guide includes a first guide arm extending from a first end to a second end on a first longitudinal axis. The first guide arm defines a first plurality of openings sized and configured to receive a first guide element therethrough. A second guide arm extends from a first end to a second end on a second longitudinal axis. The second guide arm defines a second plurality of openings sized and configured to receive a second guide element therethrough. A pivot element couples the first end of the first guide arm to the first end of the second guide arm such that an angular distance between the first guide arm and the second guide arm can be adjusted in a first plane.

Abstract: A surgical instrument having a first assembly with a first radio-opaque portion providing a profile of a first portion of an intramedullary implant or canal in a bone, and a second assembly having a second radio-opaque portion providing a profile of a second portion of the intramedullary implant or canal. The surgical instrument may also include a third radio-opaque portion providing an alignment feature to provide a fluoroscopic planar check for the surgical instrument.

Abstract: A humeral cut guide member for resectioning or resurfacing a humeral head, including a bone-engagement member including a first patient-specific bone-engagement surface that is complementary and made to substantially mate and nest in only one position on a specific patient's humeral head; a registration member connected to the bone-engagement member including a second patient-specific bone engagement surface that is sized and made to substantially mate and nest in only one position with the specific patient's bicipital groove; and a cut guide plate connected to the bone-engagement member and defining an elongated slot.

Abstract: Described are methods, systems, devices for facilitation of intraluminal medical procedures within the neurovasculature. A catheter advancement device includes a flexible elongate body having a proximal end, a distal end, and a single lumen extending therebetween. The flexible elongate body has a proximal segment, an intermediate segment, and a tip segment. The proximal segment includes a hypotube coated with a polymer. The intermediate segment includes an unreinforced polymer having a durometer of no more than 72D. The tip segment is formed of a polymer different from the intermediate segment and has a durometer of no more than about 35D and a length of at least 5 cm. The tip segment has a tapered portion that tapers distally from a first outer diameter to a second outer diameter over a length of between 1 and 3 cm.

Abstract: A medical retrieval device for retrieving stones, calculi, and the like from various organs and passages may comprising an elongated member, and a first wire and a second wire that forms a retrieval basket. The wires forming the basket and the elongated member may be secured by a crimp joint and a second joint. Processing of the device may include placing all ends of the first wire and the second wire into an elongated member through a distal end of the elongated member, moving said elongated member to a position where the first loop and the second loop start their curvatures, placing said first and second wires and said elongated member through a crimping fixture having thru cuts configured for the interlocked wires, aligning said elongated member in a desired position, and crimping said first and second wires and said elongated member.

Abstract: An ultrasonic processing apparatus is provided. The ultrasonic processing apparatus comprises an ultrasonic therapy transducer (ATA) adapted to generate focused ultrasonic waves; an ultrasonic imaging transducer (UID) connected to the ultrasonic therapy transducer; and an electronic system configured to control the ultrasonic therapy transducer so as to emit a pulse train of ultrasonic waves generating a cloud of cavitation bubbles (BC); control the ultrasonic imaging transducer so as to acquire at least one image of the region to be processed; acquire a plurality of echo signals of ultrasonic wave pulses emitted by the ultrasonic therapy transducer captured by the ultrasonic imaging transducer; process the plurality of echo signals so as to reconstruct an image of the cloud of cavitation bubbles; and display said image of the cloud of cavitation bubbles superposed on said image of the region to be processed. The processing includes spatio-temporal filtering.

Abstract: A control unit for a medical instrument is provided. The control unit includes a housing having a curved top surface capable of accommodating a hand of the user, the housing being attachable to the medical instrument. The control unit further includes a first interface engageable by a purlicue of the hand for controlling a first function of the medical instrument and a second interface engageable by one or more fingers of the hand for operating at least a second function of the medical instrument.

Abstract: Systems and methods for controlling clinical soil are provided. A system includes a device cover formed of a flexible polymer sheet defining an interior volume for a skin grafting device, and includes at least a first opening configured to receive a portion of the skin grafting device. The system further includes a cincture having a gasket configured to be affixed to a perimeter of the first opening of the device cover and to secure the device cover about the first opening to the skin grafting device to inhibit fluid ingress into the interior volume of the device cover during a skin grafting process performed using the skin grafting device.

Abstract: A discectomy device for clearing material out of a disc space of a patient having a body, a first rotatable member at the distal portion of the body, and a second rotatable member at the distal portion of the body spaced from the first rotatable member. A transverse axis passes through the first and second rotatable members. A first mechanism is actuable to rotate the first and second rotatable members about the transverse axis. A mechanism can be provided to expand the rotatable members to increase the distance between the rotatable members. The rotatable members in some versions can be detached from the device for placement within the disc space.

Abstract: Surgical tool systems and methods of use thereof for performing endoscopic surgical procedures, which systems include a handpiece and a surgical accessory which detachably connects to the handpiece. The surgical accessory has a distal end which defines a cutting head incorporating two different types of tissue-treating areas.

Abstract: Disclosed is a system to power a tool. The tool may be powered in a selected manner that may have irrigation and/or coolant provided therewith. The irrigation and cooling fluid may be provided at substantially at a working end and/or distal end of the instrument assembly.

Abstract: Systems, apparatus and methods for removing tissue of various densities from a surgical site in a minimally invasive manner are provided. The invention may include a fine stream of sterile saline, coupled with a suction effect to cut and remove tissue. A power console may be coupled with a handpiece. The power console may utilize an electric motor, thereby transmitting pressurized sterile saline through a high-pressure tube. The distal end may deliver the saline across a window as a high velocity jet stream which, when coupled with the pressure gradient, pulls and then cuts the target tissue into the cutting window and removes it. The tissue and waste saline may then travel down an evacuation lumen to a waste container. By adjusting pressures, tissue types of various densities may be debrided while minimizing disturbance of surrounding tissue.

Abstract: A transection device including a hollow tubular body extending from a proximal end to a distal end. A plurality of stabilizing members extend from the distal end of the tubular body and define a reduced diameter opening into a receiving chamber adjacent the distal end of the tubular body. A blade is positioned within the tubular body and moveable between an initial position within the tubular body to an extended position wherein at least a portion of the blade extends into the receiving chamber. A depressible member extends from the proximal end and is configured to move the blade between the initial position and the extended position. A compression member may be positioned between the plunger member and the blade.

Abstract: Surgical hub systems are disclosed. A surgical hub system comprises a surgical hub configured to communicably couple to a modular device comprising a sensor configured to detect data associated with the modular device and a device processor. The surgical hub comprises a hub processor, a hub memory coupled to the hub processor. The surgical hub system also comprises a distributed control system executable at least in part by each of the device processor and the hub processor. The distributed control system is configured to: receive the data detected by the sensor; determine control adjustments for the modular device according to the data; and control the modular device according to the control adjustments. When in a first mode, the distributed control system is executed by both the hub processor and the device processor. In a second mode, the distributed control system is executed solely by the device processor.

Abstract: A coring device, for forming an opening in a tissue wall, includes a body having a proximal end, a distal end and an internal housing, a coring head having a transection blade and being movable between a rest position and an actuated position, an actuation mechanism for moving the head between the positions and having an actuation rod, at one end of which the head is placed, a lumen extending through at least the proximal end of the body, actuation rod and coring head in order to allow passage of a flexible guide element, and the distal end of the body forms a support for a surgical tool configured to receive a hollow surgical tool with a positive fit and to support this tool to permit linear guiding of the surgical tool during the movement of the latter toward the outside of the coring device.

Abstract: Various systems and methods for controlling an ultrasonic surgical instrument according to the location of tissue grasped within an end effector are disclosed. A control circuit can be configured to apply varying power levels, via a generator, to an ultrasonic transducer driving an ultrasonic electromechanical system to oscillate an ultrasonic blade. Further, the control circuit can measure impedances of the ultrasonic transducer corresponding to the varying power levels and determine a location of tissue positioned within the end effector according to a difference between the impedances of the ultrasonic transducer relative to a threshold.

Abstract: An ultrasonic surgical instrument includes a first modular assembly including at least one operator input feature an ultrasonic transducer supported by the first modular assembly, and a second modular assembly configured to be removably coupled with the first modular assembly. The second modular assembly includes at least a portion of an end effector extending distally from a distal end portion of the second modular assembly. The instrument includes a mechanical lockout assembly configured to switch between at least an unlocked configuration and a locked configuration. In the locked configuration, the first modular assembly and the second modular assembly are partially coupled together such that the operator is physically prevented from activating the instrument using the operator input feature. In the unlocked configuration, the first modular assembly and the second modular assembly are completely coupled together and the operator is able to activate the instrument using the operator input feature.

Abstract: In an example, a scoring device is configured for retention of a catheter shaft. The scoring device incudes a proximal portion and a distal portion. A retention sleeve extends between the proximal and distal portions. The retention sleeve has a catheter socket configured to selectively receive and mechanically engage the catheter shaft. The scoring device includes a scoring tool coupled with the retention sleeve, for instance proximate to the distal portion. The scoring tool includes a balloon socket configured to selectively receive a balloon of the catheter shaft. The scoring tool includes one or more scoring elements extending around the balloon socket, the one or more scoring elements configured to provide localized scoring to vasculature.

Abstract: A device to access interior body regions includes a grippable handle, a cannula having a proximal end and a distal end, a retractable obturator disposed within the cannula and extending prominently of the distal end of the cannula, the retractable obturator being spring-biased away from the proximal end of the cannula and having an axially-extending lateral slot that is open at a distal end of the obturator and an arrow-headed blade received within the slot of the obturator, the blade being exposed only when the obturator is urged toward the proximal end of the cannula, the blade having a tip with an edge-to-edge angle in a range of 30° to 50°. The cannula is selectively securable to a blade subassembly at a distal end of the grippable handle by a hub that can be decoupled from the device by pressing a cannula/hub release button of the blade subassembly.

Abstract: Patient-mounted retractors with varying configurations and/or features are provided, along with additional components for use therewith in provided patient-mounted retractor assemblies. Blade type and tube type patient-mounted retractors that may be re-positioned during the course of a procedure are provided in varying configurations and/or geometries suitable for vayring procedures and/or patient anatomies. Applications of re-positionable patient-mounted retractor assemblies are particularly suitable for use in minimally invasive procedures, eliminating the need for table-mounted retraction assemblies and/or cannulas that restrict the operating envrionment.

Abstract: A surgical access assembly includes a surgical syringe and a balloon trocar. The balloon trocar has a collar in fluid communication with a balloon. The collar has a check valve configured to control the passage of inflation medium to and from the balloon. The syringe has a barrel and a plunger. The barrel of the syringe has a tip configured for engaging the check valve to discharge the inflation medium into the balloon. The syringe has a lateral extension configured for receipt in the check valve for opening the check valve to rapidly discharge inflation medium from the balloon.

Abstract: Catheter-based delivery systems for delivery and retrieval of a leadless pacemaker include features to facilitate improved manipulation of the catheter and improved capture and docking functionality of leadless pacemakers. Such functionality includes mechanisms directed to deflecting and locking a deflectable catheter, maintaining tension on a retrieval feature, protection from anti-rotation, and improved docking cap and drive gear assemblies.

Abstract: A nasal valve implant delivery system includes a delivery tool having a handle and a needle extending distally therefrom and configured to hold an implant therein. When loaded in the needle, the implant proximally abuts or is disposed adjacent to a pusher member disposed partially within the needle. A light source disposed within the delivery tool is coupled to an optical fiber carried within a lumen of the pusher member. The delivery tool includes a moveable needle shuttle disposed in the handle that is coupled to the needle. An actuator disposed in the handle is configured to releaseably engage with the moveable needle shuttle, wherein the needle shuttle is coupled to one or more springs configured to apply a proximal tensioning force on the needle shuttle, wherein actuation of the actuator retracts the needle proximally into the handle and releases the implant.

Abstract: Methods and devices for treatment of a uterine cavity to prevent adhesions following a surgical intervention.

Abstract: A needle assembly for harvesting human eggs, the needle assembly comprising: an outer sleeve having a proximal end and a distal end; a hollow inner needle slidably disposed within the outer sleeve and having: a distal region configured to define a curve; a distal end having a sharpened bevel; a retracted position in which the distal region is disposed within the outer sleeve; and an extended position in which the distal end of the inner needle is distal to the distal end of the outer sleeve and the distal region is at least partially external to the outer sleeve. The needle assembly further comprises a controller configured to move the inner needle between its retracted and extended positions. When the hollow needle is retracted, the distal region conforms to the outer sleeve, and when the inner needle is extended, the distal region defines the curve.

Abstract: A fracture reduction method and a parallel external fixator for fracture reduction for realizing the method, the fracture reduction method being used for existing six-chain ring-shaped parallel external fixators in minimally invasive fracture reduction or osteotomy of limbs. The parallel external fixator comprises two fixation rings, six struts and six markers, the fixation rings are arranged with a plurality of connecting holes, the struts are arranged with a spherical hinge, a driving joint (1302), a quick-mounting component and a universal hinge, the markers comprise marker balls and a pin shaft. The parallel external fixator can improve the treatment accuracy, reliability and operation convenience.

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: A uniplanar bone anchor including a housing and a bone screw is provided. The lower region of the housing defines mating elements that mate with engaging elements on the bone screw to limit movement of the housing relative to the bone screw to a single plane.

Abstract: An assembly for rectifying vertebrae, comprises: two bone anchoring means intended to be implanted on a same vertebra, a triangulation bar and a connection means for connecting the triangulation bar to each bone anchoring means and for holding the bone anchoring means in a given position in order to form, with the triangulation bar connected to the bone anchoring means by means of the connection means, a rigid triangular assembly, the triangulation bar comprising an attachment area for attaching a correction instrument arranged to ensure a rigid attachment in rotation and in translation of the correction instrument on the triangulation bar.

Abstract: A bone screw for sacroiliac joint fusion is characterized by a longitudinal bone screw and a cylindrical sleeve received on a proximal end of the bone screw. The sleeve has axially extending fins or flutes on its outer surface that extend generally from one end of the sleeve to the other end of the sleeve. This feature allows the sleeve to resist reverse rotation which, in turn, aids in preventing back-out of the bone screw once installed. The bone screw has a self-tapping tip that allows the bone screw to be installed without need for a pilot hole, and self-harvesting geometry that gathers and retains bone shavings in and along the bone screw that are produced by bone screw installation for use as graft for bone fusion.

Abstract: The present invention generally relates to bone implants. More specifically, the present invention relates to bone implants used for the fixation or fusion of the sacroiliac joint and/or the spine. For example, a system for fusing or stabilizing a plurality of bones is provided. The system includes an implant structure having stem portion and a head portion, the stem portion having a rectilinear cross sectional area. A tulip or saddle structure can be attached to the head portion, and a rod can be secured within the tulip or saddle structure.

Abstract: A fluid routing system for use in an indoor grow facility includes a plurality of supply lines, and a plurality of frames aligned in series and spaced apart from each other. Each of the frames includes a plurality of support openings. Each of the support openings is sized to receive and retain a corresponding one of the supply lines.

Abstract: The present invention is a system or implant adapted for use in bone cavities. The current system is particularly useful in surgical procedures involving fractured bones.

Abstract: Implant systems in some embodiments such as midline incision implant systems may generally include an insertion guide assembly and a plate, which define fixation trajectories. In other embodiments such as a percutaneous implant system may generally include a first a plate, an insertion guide, and a separate second insertion guide, which define fixation trajectories. Surgical methods include use of the implant systems with the plates, and use of plates alone, for installing bone fusion systems.

Abstract: The device is a tibial plateau leveling osteotomy (TPLO) plate is used to stabilize a stifle joint in an animal in veterinary surgery after a torn cranial cruciate ligament. The TPLO plate has a proximal portion and a distal portion, connected by an offset portion.

Abstract: A bone fixation system includes a length of suture, a screw, a tensioning tab, and an anchor. The length of suture has a first end and a second end. The screw comprises an elongated shaft having a threaded external surface, wherein the screw has a distal end, a proximal end, and an internal surface defining a passageway within the screw extending between the distal end and the proximal end, wherein the passageway is configured to receive the length of suture. The tensioning tab is affixed to a section of the length of suture. The anchor is configured to secure the first end of the length of suture adjacent to the proximal end of the screw.

Abstract: A bone screw cutting system can include a cutting assembly having a plurality of blades. The system can further include a position adjustment assembly coupled to the cutting assembly and configured to receive a bone screw blank and position the bone screw blank relative to the cutting assembly. The cutting assembly is configured to cut a bone screw blank received by the position adjustment assembly and to form a self-tapping end portion at a cut end of a resulting cut bone screw.

Abstract: A bone fastener includes a screw shaft having a proximal portion and a distal portion. The proximal portion is formed by a first manufacturing method and defines a distal face. The distal portion is formed onto the distal face by a second manufacturing method. In some embodiments, systems, spinal constructs, surgical instruments and methods are disclosed.

Abstract: A medical balloon device includes an outer member extending along an axis. An inflatable member has a proximal end extending from a first end of the outer member and a distal end. An inner member is positioned within the outer member and the inflatable member such that a first end of the inner member is coupled to the distal end of the inflatable member. A support member is movably disposed within the inner member and includes a first end configured to removably engage the first end of the inner member. Translation of the support member along the axis causes the inflatable member to move between a first position in which the inflatable member has a first length and a first profile and a second position in which the inflatable member has a second reduced length and a second reduced profile. Methods of use are disclosed.

Abstract: The present invention proposes an apparatus and method for estimating a level of thermal ablation. The apparatus (110) comprises a data interface (111) configured to receive the three-dimensional ultrasound echo data of the tissue region; and a data processor (113) configured to measure in-plane strain and out-of-plane motion regarding the tissue region on basis of the received ultrasound echo data. The data processor (113) is further configured to estimate the level of tissue ablation for the tissue region on basis of the in-plane strain, the out-of-plane motion, and a predetermined model, and the predetermined model at least reflecting a first causal relationship between the in-plane strain and the level of tissue ablation and a second causal relationship between the out-of-plane motion and the level of tissue ablation.

Abstract: A surgical instrument comprises a shaft assembly comprising a shaft and an end effector coupled to a distal end of the shaft; a handle assembly coupled to a proximal end of the shaft; a battery assembly coupled to the handle assembly; a radio frequency (RF) energy output powered by the battery assembly and configured to apply RF energy to a tissue; an ultrasonic energy output powered by the battery assembly and configured to apply ultrasonic energy to the tissue; and a controller configured to, based at least in part on a measured tissue characteristic, start application of RF energy by the RF energy output or application of ultrasonic energy by the ultrasonic energy output at a first time.