Abstract: A surgical severing and stapling instrument, suitable for laparoscopic and endoscopic clinical procedures, clamps tissue within an end effector of an elongate channel pivotally opposed by an anvil. Various embodiments are configured to be operably attached to a robotic system to receive actuation/control motions therefrom.

Abstract: A detachable motor-powered surgical instrument. The instrument may include a housing that includes at least one engagement member for removably attaching the housing to an actuator arrangement. A motor is supported within the housing for supplying actuation motions to various portions of a surgical end effector coupled to the housing. The housing may include a contact arrangement that is configured to permit power to be supplied to the motor only when the housing is operably attached to the actuator arrangement.

Abstract: Devices and methods for deploying an anastomotic stent between portions of the gastrointestinal (GI) tract are disclosed. The anastomotic stents are configured to atraumatically engage the tissue walls and to permit the flow of fluid, partially digested food, and food. The stents can be deployed using endoscopic catheter devices, laparoscopic tools, and combinations of both endoscopic tools and laparoscopic tools. Examples of anastomoses include anastomoses between the stomach and a portion of the intestines such as the jejunum. Anastomoses can also be formed between two closed ends of the intestines, such as two closed ends of the colon formed during a colon resection procedure. Anastomoses can also be formed between a fundal pouch formed during a gastric bypass procedure and the jejunum. Laparoscopic tools are disclosed to deploy a stent by selectively removing a radial restraint on a self expanding stent with the restraint removed through the laparoscopic access points.

Abstract: A surgical stapling device includes a handle assembly that supports an audible indicator mechanism including a spring biased clicker. The spring biased clicker includes a pin that is received within a pin slot or cavity in the housing of a stationary handle of the handle assembly. The pin is movable through the cavity in response to actuation of the firing trigger assembly and unapproximation of the anvil assembly to guide movement of the clicker such that the clicker 1) provides an enhanced audible indication to a clinician that the firing stroke of a firing trigger has been completed, and 2) provides an enhanced indication to a clinician that the anvil assembly has been moved back to the unapproximated or spaced position after the firing stroke has been completed.

Abstract: Tissue ligation devices and methods are provides to mechanically strangulate abnormal or undesirable tissue. Tissue ligation devices include a catheter having an outer diameter smaller than the inner diameter of a standard endoscope channel such that the catheter can be inserted into the endoscope. Tissue ligation devices also include a ligation system with an expandable hood disposed located at the distal end of the catheter. A suture extends through a lumen of the catheter and has a distal loop portion exposed outside of the expandable hood.

Abstract: A pushing apparatus and conveying system for an interventional medical instrument. By covering a thermoplastic elastomer on the surface of a steel cable to form an overlay film, steel cable support is improved when guaranteeing the flexibility thereof so that it is difficult for the instrument to deviate from a predetermined position when conveying the instrument, the operation time is shortened, and the operation risk of patients is reduced. Meanwhile, in the conveying system, a sealing member is provided in an inner cavity of a hemostasis valve body to match the overlay film of the steel cable so that the distal end of the hemostasis valve body is isolated from the outside, and the release effect of the instrument can be assessed by radiography before the instrument is released from the steel cable in operation, thereby effectively reducing harm to patients.

Abstract: A system for delivering a vascular implant into a body lumen including a vascular implant having a first engagement portion at a proximal portion and an elongated delivery member having a second engagement portion at a distal portion releasably engageable with the first engagement portion. An elongated member extends through the delivery member wherein in the extended position the elongated member extends into at least a portion of the implant to prevent release of the implant from the delivery member and in the retracted position the elongated member enables release of the implant from the delivery member.

Abstract: There are disclosed various dispensing mechanisms for dispensing filamentary material through a catheter into a treatment site of a patient, for example into an aneurysm sack in a patient's vessel. In one embodiment the assembly includes a conical material carrier which is substantially aligned with the dispensing direction, thereby avoiding the need to have a rotating carrier. Another embodiment has a carrier which is at least partially cylindrical. The carrier provides for efficient dispensation of filamentary material at substantial dispensing speeds.

Abstract: An intrasaccular flow diverter includes a wire structure (e.g., a braided wire or a laser-cut hypotube), a thin-film mesh placed over the wire structure, and crimps fixing the thin-film mesh to the wire structure at each crimp. The wire structure and the thin-film mesh between adjacent crimps are expanded radially to form thin-film covered spheroid structures. When deployed in an aneurysm, the spheroid structures may volumetrically fill the aneurysm sac. An intrasaccular flow diverter with an umbrella structure includes a wire structure with a plurality of crimps along the wire structure, and a thin-film covered umbrella structure at one end of the wire structure. The wire structure between adjacent crimps is expanded radially to form a spheroid structure. When deployed in an aneurysm, the thin-film covered umbrella structure may cover the aneurysm neck.

Abstract: Methods and apparatuses for embolizing an artery in a living subject using a catheter are disclosed. The catheter has a lumen and also has a balloon located near the distal end of the catheter. The distal end of the catheter is introduced into the artery, and the balloon is inflated to form a seal that prevents blood in the artery from flowing past the balloon. A mixture that includes embolic particles and contrast agent is injected through the lumen into the portion of the artery that is distally beyond the balloon. The subject's own blood or another fluid that contains platelets is injected through the lumen into the portion of the artery that is distally beyond the balloon. Subsequently, the balloon is deflated and the distal end of the catheter is withdrawn.

Abstract: A femur cutting jig mechanism (FCJM) is provided having a number N1 of spaced apart FCJM contact points that correspond to a number N1 of spaced apart femur contact points on at least one of a medial condyle, a lateral condyle, and a trochlear groove on the patient's knee. The FCJM contact points are positioned in contact with the knee contact points, and a cut bar mechanism is positioned in contact with the FCJM to provide a location and an angular orientation of a cut bar plane that is to be used to resection and remove a selected portion of the patient's, knee. The FCJM is removed from the patient's knee, and a selected portion of the patent's knee is resectioned and removed. The number N1 is at most 12 in some embodiments.

Abstract: Devices for treating a bone and methods of inserting such devices into a bone are disclosed. A device for treating a bone may include a flexible tube, a stiffening mechanism and an actuator. The flexible tube has a distal end and a proximal end. The stiffening mechanism within the flexible tube is configured to cause the flexible tube to become rigid. The actuator is configured to cause the stiffening mechanism to cause the flexible tube to become rigid in response to the actuator being actuated.

Abstract: A technique for accessing extra articular lesions or abnormalities or intra osseous lesions or abnormalities or bone marrow lesions or all has the step of positioning the localizing pinning member onto cartilage or subchondral bone to define a virtual pathway through the cartilage or subchondral bone towards or into or through the lesion or abnormality or a desired target to create the virtual pathway utilizing an intra articular localizing pinning member to determine a location of the lesion or abnormality wherein the utilization of the localizing pinning member includes the step to locate or stabilize or both and thereafter using the virtual pathway to create an entry access.

Abstract: Devices, systems, and methods are provided for ligament repair procedures, and can be used to establish a location and trajectory for forming a bone tunnel in bone. One exemplary embodiment of a surgical guide for using in a ligament repair procedure includes a guide arm and a carriage that can be selectively locked along the guide arm to define an angle of the bone tunnel. The guide arm also defines a location of a distal end of the bone tunnel. In some embodiments the carriage is configured to have a bullet side-loaded into it, and the bullet can be used to define a location of a proximal end of the bone tunnel. The present disclosure also provides for a gage that limits the distance a drill pin that drills the bone tunnel can travel. A variety of other, devices, systems, and methods are also provided.

Abstract: An orthopaedic surgical instrument system for use in preparing a patient's bone is disclosed. The surgical instrument includes a cutting guide block configured to be secured to a surgically-prepared surface of the patient's bone, and a cutting tool to be used in conjunction with the cutting guide block to resect a section of the patient's bone. A method of performing an orthopaedic surgery is also disclosed.

Abstract: The present invention includes a method and devices for treating osteonecrosis in, e.g., children, adolescents, and adults comprising: identifying a subject in need of treatment for osteonecrosis; drilling two or more holes into a bone in need of treatment for osteonecrosis; inserting two or more needles or cannulas into the holes in the bone; washing an interior of the bone with a washing fluid introduced through one or more of the needles or cannulas inserted into the bone; and after washing the interior of the bone introducing one or more bone growth promoting materials or cells into the bone.

Abstract: Systems and methods for joint replacement are provided. The systems and methods can include a surgical orientation device and/or a reference sensor device. The surgical orientation device and orthopedic fixtures can be used to locate the orientation of an axis in the body, to adjust an orientation of a cutting plane or planes along a bony surface, to distract a joint, to measure an angle, to orient a cutting guide, to orient a resection guide, to resect the femur, or to otherwise assist in an orthopedic procedure or procedures.

Abstract: The invention relates to an aspiration catheter for the aspiration of material from blood vessels. The aspiration catheter according to the invention comprises a tubular catheter wall (2) having a first distal opening (3) and a first proximal opening (4). These two openings (3, 4) are connected to each other by a first lumen (5). The aspiration catheter further comprises a tubular guide sleeve (6) having a second distal opening (7) and a second proximal opening (8). A second lumen (9) extends between these two openings (7, 8). The tubular guide sleeve is arranged within the first lumen (5), wherein the second lumen (9) extends coaxially to the first lumen (5). The second proximal opening (8) extends laterally through the tubular catheter wall (2). The tubular guide sleeve is connected to the tubular catheter wall (2) in a region (X) of the first distal opening (3) and in a region (Y) of the second proximal opening (8).

Abstract: Numerous devices are described. One device may comprise: a handle including a wire attachment portion; an actuator movably mounted to the handle, the actuator including a reaction chamber; a plunger movably mounted to the actuator, the plunger including a distal stop with a sheath attachment portion, and a proximal stop located in the reaction chamber; a resilient element including a distal end attached to the proximal stop, and a proximal end movable relative to plunger; and a force reduction element located in the reaction chamber between the resilient element and a reaction surface in the cavity. The resilient element may bias the plunger distally relative to the actuator, and be compressed when a proximally-directed force is applied to the plunger. The force reduction element may dissipate a portion of the proximally-directed force. Related devices and methods are also described.

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

Abstract: A medical device for the treatment of a sinus opening includes a handle, a grooming sheath, a rail, a guide wire, a balloon catheter and a balloon catheter movement mechanism. The handle has a proximal end, a distal end and a longitudinal axis along the length of the handle. The grooming sheath has a distal end and a proximal end with the proximal end of the grooming sheath being attached to the distal end of the handle. The rail has a distal end and a proximal end and disposed partially within the grooming sheath to define an annular lumen is between the rail and the grooming sheath. The guide wire operatively extends from the distal end of the rail and the balloon catheter is disposed at least partially in the handle and annular lumen.

Abstract: A needle knife device and system for cutting soft tissue under skin of a patient are provided. The needle knife can include an elongated needle including a lumen and a beveled point configured to allow the elongated needle to be inserted transcutaneously into the skin of the patient. The needle knife can also include a blade that is capable of being oscillated within the lumen of the elongated needle between a retracted position where the blade is disposed within the needle and a deployed position where the blade is disposed outside the needle beyond the beveled point. A motor unit can be operatively arranged with the blade and configured to oscillate the blade.

Abstract: A surgical instrument includes: a handpiece; a movable member configured to transmit a driving force to a treating member to treat a subject by moving relatively to the handpiece; and a connector arranged inside the handpiece, and including a strip to apply a pressing force to the movable member. The movable member includes a first conductive portion formed therein. The connector includes a second conductive portion formed on the strip. The second conductive portion abutting against the first conductive portion to connect the movable member and the handpiece electrically. The second conductive portion of the connector is a molded interconnect device constituting a three-dimensional circuit.

Abstract: An ultrasonic surgical shears includes an ultrasonic surgical blade, a clamping arm operable to open and close toward the blade, and a tissue pad attached to the clamping arm. A method for sealing a blood vessel of a patient includes obtaining an ultrasonic surgical shears and positioning the blood vessel between the blade and the tissue pad. The clamping arm is operated to exert an average coaptation pressure between and including 120 psi and 210 psi. The blade is ultrasonically vibrated to transect and seal the blood vessel.

Abstract: A method and apparatus for treating a clot in the blood vessel of a patient, and particularly the treatment of a pulmonary embolism is disclosed. The treatment includes restoring flow through the clot followed by clot removal, either partially or substantially completely. The clot treatment device is expandable into the blood vessel and may contain radial extensions that assist in restoring flow as well as in removing clot material.

Abstract: A balloon catheter is provided that may be used to dilate hardened regions of a stenosis. The balloon catheter is provided with one or more dilation elements that extend along a surface of a balloon. Each dilation element is monolithically connected to an outer surface of the balloon by a connector. The connector is sufficiently sized and designed to undergo stress-induced plastic deformation incurred during blow molding so that a significant portion of each of the dilation elements does not become absorbed into the wall of the final blow molded balloon, thereby maintaining the structural integrity of each of the dilation elements. The dilation element has a flattened outer surface along at least proximal and distal neck portions of the balloon.

Abstract: Provided are a surgery system that can ensure insulation between an endoscope and a treatment tool. The endoscope has an insertion part that is insertable into an overtube and has a distal end, a proximal end, and a longitudinal axis, and is locked to the movable body by an endoscope holding part. The endoscope has a first insertion part that is provided on a distal end side of the insertion part, a second insertion part that is provided on a proximal end side of the first insertion part and has an external diameter larger than that of the first insertion part, and a held part that is provided from a distal end of the second insertion part toward a proximal end side thereof, is held by the endoscope holding part, and has at least a surface formed of an insulating member having an insulation property.

Abstract: Methods, systems, and compositions are provided for implanting an implantable device into a biological tissue (e.g., muscle, brain). A subject implantable device includes: (i) a biocompatible substrate, (ii) a conduit (e.g., an electrode, a waveguide) that is disposed on the biocompatible substrate, and (iii) an engagement feature (e.g., a loop) for reversible engagement with an insertion needle. The biocompatible substrate can be flexible (e.g., can include polyimide). The implantable device is implanted using an insertion needle that includes an engagement feature corresponding to the engagement feature of the implantable device. To implant, an implantable device is reversibly engaged with an insertion needle, the device-loaded insertion needle is inserted into a biological tissue (e.g., to a desired depth), and the insertion needle is retracted, thereby disengaging the implantable device from the insertion needle and allowing the implantable device to remain implanted in the biological tissue.

Abstract: The present invention includes a method and devices for treating osteonecrosis in, e.g., children, adolescents, and adults comprising: identifying a subject in need of treatment for osteonecrosis; drilling two or more holes into a bone in need of treatment for osteonecrosis; inserting two or more needles or cannulas into the holes in the bone; washing an interior of the bone with a washing fluid introduced through one or more of the needles or cannulas inserted into the bone; and after washing the interior of the bone introducing one or more bone growth promoting materials or cells into the bone.

Abstract: Systems for insufflation and recirculation of insufflation fluid in a surgical procedure include a control unit having a fluid pump, a supply conduit, a return fluid conduit and a pressure-controlled valve. The pressure-controlled valve is in fluid communication with an insufflation gas supply, the supply conduit and the return conduit and is adapted and configured to respond to pressure control signals to adjust position and thereby system flow parameters, to reduce entrainment of air from the surrounding environment, and to increase the concentration of insufflation gas in an operative space, and/or to reduce an overpressure condition in the operative space.

Abstract: Pair of dynamic external fixation devices (100) for the reduction of fractures of bone fragments, said devices (100) being arranged on either side of a first bone portion traversed by a first pin (10) in a proximal position and a second bone portion traversed by a second pin (11) in distal position, while each of the dynamic external fixation devices (100) includes a first body (1) having a longitudinal axis profile (X, X?), having a proximal bore (5) passing through an axis (Y, Y?) in combination with the first pin (10), said first body (1) being embedded in a first coil spring (8), while said first spring (8) is nested in a second coil spring (12), mounted in conjunction with a second body mounted in conjunction on said first body (1), while the second body is mounted in conjunction with the second pin (11).

Abstract: A skull fixing device includes at least a lower fastening member and a movable retainer assembly. The lower fastening member includes a thread rod having a first coupling section formed in an interior thereof. The movable retainer assembly includes at least an upper fastening member and a nut. The upper fastening member includes a sleeve section in which a first rotation section is formed. The nut is screwed to the threaded rod and has an upper end forming a first positioning section and has an outer surface forming a second rotation section mating the first rotation section. Also disclosed is a surgery tool that includes at least a outer barrel having a lower end forming a second positioning section engageable with the first positioning section and an inner guide rod having a lower end forming a second coupling section engageable with the first coupling section.

Abstract: A method of limiting at least one degree of movement between a superior vertebral body and an inferior vertebral body of a patient includes advancing a distal end of a stabilization device into a pedicle of the inferior vertebral body. A proximal portion of the stabilization device is positioned such that the proximal portion limits at least one degree of movement between a superior vertebral body and an inferior vertebral body by contacting a surface of the superior vertebral body.

Abstract: A closure for an open headed medical implant, such as a bone screw. The closure having a cylindrical body having an axis of rotation and also having a radially outer surface with a thread or other guide and advancement structure thereon. The body having a plurality of apertures that open onto a top surface of the body and that are parallel to but spaced from the axis of rotation. The closure also has a break-off head centrally attached by a neck to the top surface of the body.

Abstract: A device (1) for fixating a rod (10) on a bone with a tulip, with a pedicle screw (2) and with a tightening screw (5). The rod clamp (6) is pivotable to the tightening screw and can follow transverse motions of the rod (10). This increases the stability of the entire structure, particularly in the application in spine surgery.

Abstract: The present application generally relates to orthopedic stabilization systems, and in particular, to systems including clamps. The clamps can be used in addition to or to replace hooks that grasp onto bone members, such as the lamina. One example of such a clamp is an in-line clamp that includes a central opening for receiving a rod member, a first opening for receiving a set screw and a second opening for receiving an elastic member therethrough. Another example of such a clamp is an off-set clamp that includes an upper plate, a bottom plate, and an opening for receiving a rod therein. The upper plate can be separated from the bottom plate to make space for an elastic member that can be secured within the plates. Tulip clamps that utilize one or more elastic members are also provided.

Abstract: A spinal distractor for distracting opposed vertebrae in which a pair of elements are threadably connected by a screw having opposing threads, wherein actuating the screw spreads the elements apart and pushes the vertebrae apart.

Abstract: Embodiments herein are generally directed to derotation systems, apparatuses, and components thereof that can be used in spinal derotation procedures, as well as methods of installation. The derotation systems may include a plurality of derotation towers and clamp members.

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: Apparatus and devices for percutaneously extending an existing spinal construct ipsilaterally with an additional spinal construct in a patient are disclosed. The additional spinal construct comprises a rod connector that includes an elongate additional rod integrally attached thereto. The additional rod is placed through an access port in a first orientation generally parallel to the longitudinal axis of the access port and rotated to a different second orientation generally transverse to the longitudinal axis of the access port. During such rotation the additional rod is moved subcutaneously beneath the skin of the patient from the existing spinal rod to an additional bone engaging implant. In another arrangement, the extension of an existing spinal construct in a minimally invasive procedure comprises a rod connector having an offset support for receiving an additional spinal rod that may be placed laterally interiorly or exteriorly of the existing spinal construct.

Abstract: A system, and method of using the system, for changing the angle of a bone of a subject is provided by the present disclosure.

Abstract: Assemblies and methods for fixation of bone or bone fragments using an orthopedic plate, a modular peg, and a compression screw. The modular peg is screwed into one of the apertures of the orthopedic plate. The modular peg may include an aperture having screw threads designed to receive the threads of the compression screw and serve as an anchor for the compression screw. By rotating the compression screw in relation to the modular peg, the compression screw may advance through the aperture of the modular peg, drawing the head of the screw toward the modular peg, and compressing the bone or bone fragments.

Abstract: Invention is related to the nails used in the surgical treatment of humeral fractures. And it is characterized with, humerus internal safe locking nail (1) which is including; Locking pin (2) providing distal locking by outgoing from the distal hole of the nail (8) in pursuit of being screwed inside all along from the proximal of the humerus internal safe locking nail (1) At least one locking sending slot (3) on the locking pin (2) providing locking pin (2) to be sent to lock from the distal part At least one locking pin slot of the nail (5) on the proximal part of the humerus internal safe locking nail (1) providing locking pin (2) to proceed into humerus internal safe locking nail (1).

Abstract: A bone plate system is provided that permits rapid, secure stabilization of a plurality of bones, such as portions of a cut rib. The bone plate system includes a bone plate having anchor devices for securing the bone plate to, for example, cortical bone of the cut rib portions. The anchor devices have an open configuration that permits the anchor devices to be connected to the cortical bone of the cut rib portions and a clamping configuration that fixes the bone plate to the cortical bone of the cut portions. The bone plate connects the cut rib portions and stabilizes the cut rib portions against relative movement therebetween.

Abstract: An extreme movement osteotomy device includes an attachment plate suitable for being locked to the cortical substance of the bone to be treated, having a first proximal portion suitable for being attached to the inner cortical substance of the metatarsal diaphysis of the bone, a distal portion suitable for being attached to the outer cortical substance, next to the epiphysis of the metatarsus, and a central portion connecting the proximal and distal portions, each one of the proximal and distal portions of the plate being provided with at least one hole and orthopaedic screws to pass therethrough; and a proximal intramedullary support system having a shank with a foam tip extending from the end of the proximal portion of the plate.

Abstract: The present invention relates to a surgical screw capable of self-locking and a fusion device using the same. The screw includes: a screw body having a body main thread formed on an outer circumferential surface thereof, a body locking thread spaced apart from the body main thread with an offset portion interposed therebetween, and a body driving groove formed in the upper portion thereof; and a sleeve having a sleeve thread formed on an inner circumferential surface thereof to be screwed with the body locking thread, and a sleeve stopper spaced downwards from the sleeve thread so as to support the body locking thread. The surgical screw may also be included in a fusion device in a different form by coupling with a plate or a cage.

Abstract: Described herein are devices, systems and methods for treating disease and/or infection by the release of silver from an implant over an extended period of time. In particular, the devices described herein may be used to treat infections such as osteomyelitis by the controlled release of silver ions from multiple sites of an extended-use implant. This implant typically includes a plurality of arms that both anchor and help distribute the released ions within the tissue. Power may be applied to release the silver ions into the tissue.

Abstract: An ablation needle device is a needle device intended for an ablation treatment of an adrenal tumor with transvenous introduction of an injection needle into an adrenal gland. The ablation needle device includes a metal injection needle including a pointed tubular distal portion and a tubular proximal portion, and a grip portion attached to a proximal side of the injection needle. The proximal portion of the injection needle is given flexibility by forming a helical slit in a distal region of the proximal portion. An outer surface of the proximal portion is coated with resin. A distal end of the distal portion of the injection needle is closed. A plurality of fine holes are formed in an outer surface of the distal portion including the closed part. The grip portion has a liquid-injection port for supplying liquid into the lumen of the injection needle.

Abstract: Endolumenal devices and methods can be used for the treatment of health conditions including obesity and diabetes. In some embodiments, the methods and systems provided herein can cause weight loss or control diabetes by reducing the caloric absorption of an individual. For example, this document provides several devices and methods for treating obesity and diabetes by using electroporation to modulate the duodenal mucosa. In addition, this document provides devices and methods for bypassing portions of the gastrointestinal tract to reduce nutritional uptake.

Abstract: A control device controls a surgical instrument including a heater. The control device includes a first power supply, a second power supply, a resistance value calculation section, and an output control circuit. The first power supply outputs a first current having a first frequency and supplied to the heater. The second power supply outputs a second current combined with the first current, supplied to the heater and having a second frequency different from the first frequency. The resistance value calculation section separates a signal component related to the second current from the first and second currents having passed through the heater, and calculates a heater resistance value based on the signal component. The output control circuit controls a temperature of the heater based on the heater resistance value.