Abstract: Disclosed are devices for pericardial access to the heart, including direct access to the left atrium. In certain embodiments, the device may comprise a device and/or an atrial appendage (AA) portal having a configuration such that the distal end of the device and/or the portal can access an atrial appendage while the proximal end of the device and/or portal can extend to outside of the subject. The devices and methods may also include a pericardial portal for emplacement of the device and/or the AA portal. Also, methods for using such devices and/or AA portals and pericardial portals to perform surgery on the heart, and systems (e.g., kits) comprising these devices and/or portals in combination with other therapeutic devices are disclosed.

Abstract: The device comprises a clamp secured to a cutting guide (4) and comprising two arms (1) and (2) articulated against an elastic return means (3).

Abstract: A measurement system and method for determining a depth of penetration of a working portion of a surgical instrument (e.g., a rotating drill bit in a bore). A first sensor outputs a first signal representative of a displacement of the leading edge of the drill bit in the bore. A second sensor outputs a second signal representative of a force applied to the leading edge of the drill bit. A processor outputs a third signal representative of the depth of penetration of the leading edge of the drill bit when the leading edge of the drill bit passes from a first medium having a first density to a second medium having a second density. The third signal is based on the first and second signals.

Abstract: A kit including a guiding system and a bone material removal device, including an arcuate element, a guiding element configured to be attached to the arcuate element, a cannula, slidably insertable into a portion of the arcuate element, a cannulated bone material removal device having a longitudinal shaft, which is axially displaceable within the cannula.

Abstract: A surgical drill guide for positioning, aligning, and of holes to be drilled in bone tissue has retaining means that holds the position and alignment of the drill guide body in a releasable manner with respect to a fastener hole in an orthopedic implant. The retaining means is a key guide that mates with a key way or key ways in or around a threaded locking hole of an orthopedic plate for alignment of a pilot hole and method of using the guide. The key guide has 2 to 8 projections that extend in the direction of the axis of the hole, such as hemi cylindrical projections, and the plate has a corresponding female key way that receives the retaining means. The invention also relates to a method of aligning a locking fastener in a plate at a desired angle relative to a bone by using a surgical guide having a key interface with the plate to position and align a pilot hole.

Abstract: An orthopedic surgical instrument includes from about 40 wt % to about 85 wt % of a base thermoplastic and from about 15 wt % to about 60 wt % of a filler material. The base thermoplastic includes polyetherimide, polycarbonate, modified polyphenylene ether, polyamide, copolymers of these thermoplastics, and combinations thereof. In some aspects all materials in the orthopedic surgical instrument are biocompatible. An orthopedic surgical kit includes an orthopedic surgical instrument and a container suitable for sealing the orthopedic surgical instrument therein. The orthopedic surgical instrument in the kit includes from about 50 wt % to about 90 wt % of a base thermoplastic selected from the group consisting of polyetherimide, polycarbonate, modified polyphenylene ether, polyamide, copolymers of these thermoplastics, and combinations thereof, and from about 10 wt % to about 50 wt % of a filler material.

Abstract: A method for performing an orthopaedic surgical procedure on a knee joint of a patient includes resecting a proximal end of a patient's tibia to create a resected surface of the patient's tibia and positioning a tibial paddle of a sensor module on the proximal end of the patient's tibia. The tibial paddle includes a sensor array generating sensor signals indicative of the joint force of the patient's knee joint. The method also includes performing a number of orthopaedic surgical steps while monitoring a display of the sensor module that provides a visual indication of the medial-lateral balance of the joint force of the patient's knee joint.

Abstract: A retrieval medical device for entrapping and retaining an object located in a body for its extraction therefrom is described. The device includes a basket-filter constituted by a plurality of filaments extending from the proximal end towards the distal end. The filaments are bound together in the vicinity of the proximal end to form a plurality of main branches. Each main branch includes at least two filaments. The filaments are entangled together in the vicinity of the distal end. Each main branch has a ramification point at which it ramifies into at least two single filaments extending from the ramification point towards the basket distal end of the basket-filter. One of the single filaments extends in the form of a right spiral, whereas another single filament extends in the form of a left spiral. The filaments extending from the ramification points interlace with each other, thereby forming a mesh between the branching point and the basket proximal end having density greater than 5.

Abstract: Disclosed herein are ultrasonic probes and systems incorporating the probes. The probes are configured to produce an ultrasonic therapy exposure that, when applied to a kidney stone, will exert an acoustic radiation force sufficient to produce ultrasonic propulsion. Unlike previous probes configured to produce ultrasonic propulsion, however, the disclosed probes are engineered to produce a relatively large (both wide and long) therapy region effective to produce ultrasonic propulsion. This large therapy region allows the probe to move a plurality of kidney stones (or fragments from lithotripsy) in parallel, thereby providing the user the ability to clear several stones from an area simultaneously. This “broadly focused” probe is, in certain embodiments, combined in a single handheld unit with a typical ultrasound imaging probe to produce real-time imaging. Methods of using the probes and systems to move kidney stones are also provided.

Abstract: Various embodiments are direct to a surgical instrument comprising and end effector, an articulating shaft and an ultrasonic transducer assembly. The end effector may comprise an ultrasonic blade. The articulating shaft may extend proximally from the end effector along a longitudinal axis and may comprise a proximal shaft member and a distal shaft member pivotably coupled at an articulation joint. The ultrasonic transducer assembly may comprise an ultrasonic transducer acoustically coupled to the ultrasonic blade. The ultrasonic transducer assembly may be positioned distally from the articulation joint.

Abstract: According to some embodiments, a method of treating a skin surface of a subject comprises heating a skin surface, abrading native skin tissue of a subject using a microdermabrasion device, wherein using the microdermabrasion device comprises moving the microdermabrasion device relative to the skin surface while simultaneously delivering at least one treatment fluid to the skin surface being treated and cooling the abraded skin surface.

Abstract: A surgical handpiece includes a housing gripped by a user, and an aspiration pipe that is attachably and detachably held by the housing and aspirates a liquid.

Abstract: A system to treat a patient comprises a user interface that allows a physician to view an image of tissue to be treated in order to develop a treatment plan to resect tissue with a predefined removal profile. The image may comprise a plurality of images, and the planned treatment is shown on the images. The treatment probe may comprise an anchor, and the image shown on the screen may have a reference image marker shown on the screen corresponding to the anchor. The planned tissue removal profile can be displayed and scaled to the image of the target tissue of an organ such as the prostate, and the physician can adjust the treatment profile based on the scaled images to provide a treatment profile in three dimensions. The images shown on the display may comprise segmented images of the patient with treatment plan overlaid on the images.

Abstract: The Powerline Communication (“PLC”) systems and methods described allow for bi-directional communication along an AC or DC conductor between a first device and at least a second device comprising a medical device system. Generally, two devices within a sterile field may communicate with each other by PLC or a first device within a sterile field may communicate with a second device that is outside the sterile field by PLC. More specifically, a controller unit may communicate with a saline, or other fluid, pump to achieve a variety of functional purposes. Similarly, a measurement device may share measured data with another device.

Abstract: An energy treatment instrument includes a held unit capable of being held, and an electric-receiver-side resonator including an electric receiver coil wound around a coil axis, and resonating at the same resonance frequency as an electric-supplier-side resonator, thereby electric power being supplied from an electric supplier coil to the electric receiver coil. The energy treatment instrument includes an energy generator generating energy for use in a treatment by using the electric power supplied to the electric receiver coil, and a magnetic member including a magnetic material and located distant from the coil axis of the electric receiver coil.

Abstract: Disclosed is an amputator, which is provided at one end of a transmitting rod connected to a vibrator generating ultrasonic waves, for amputating a surgical site by means of ultrasonic waves transmitted from the transmitting rod, the amputator comprising: an amputating side which comes in contact with the surgical site; and a direction switching means, which has a depression in one part thereof from a point corresponding to a vibration node, for concentrating the ultrasonic waves on the amputating side, the ultrasonic waves being transmitted at an angle toward the amputating side along the lengthwise-direction.

Abstract: An ultrasonic surgical system has an ultrasonic unit including an instrument operatively connected to an ultrasonic generator, wherein the instrument has an ultrasonic end effector on the distal end of a shaft. The system further includes a positioning unit including a movable arm adapted for releasably holding the instrument, whereby an operator may direct the positioning unit to position the end effector at a surgical site inside a body cavity of a patient for performing a plurality of surgical tasks. The system further includes a control unit operatively connected to the ultrasonic and positioning units, wherein the control unit is programmable with a surgical subroutine for performing the surgical tasks. The system further includes a user interface operatively connected to the control unit for initiating an operative cycle of the surgical subroutine such that the surgical tasks are automatically performed during the operative cycle.

Abstract: A dilator that facilitates implantation of an interspinous spacer is provided. The dilator includes a proximal portion and a tapered distal portion interconnected by an elongated body portion. The tapered distal portion is ideally suited for splitting ligamentous tissue for creating a posterior midline pathway through the supraspinous ligament as well as for distracting the adjacent spinous processes. Two oppositely located and longitudinally extending channels or grooves are formed in the outer surface of the dilator for stabilizing the dilator with respect to the spinous processes. An accompanying cannula together with the dilator form a system for the distraction of the adjacent spinous processes, stabilization of the spinous processes with respect to the system and creation of a working channel for the implantation of an interspinous spacer.

Abstract: The present disclosure relates to a guide assembly. The guide assembly includes a guide having a body having a first set of marks and a joint including at least one through hole, the joint configured for sliding along the length of the body; and a first surgical device having a second set of marks, wherein the guide is coupled to the first surgical device and a longitudinal axis of the through hole is co-radial with a mark of the second set of marks when the joint is located at a mark of the first set of marks. Other guides are also disclosed.

Abstract: A transseptal needle or punch wherein the distal end of the transseptal needle is able to articulate laterally out of the longitudinal axis of the steerable transseptal needle. The transseptal needle further comprise a blunted distal end configuration that is minimally traumatic. Under control by the user or a computer, at the proximal end of the transseptal needle can be articulated to generate various curves with high bending force. The transseptal needle is configured for use within a transseptal introducer.

Abstract: An apparatus is provided for use in a medical procedure for stabilizing a target during approach of the apparatus towards the target. The apparatus comprises a body having a proximal end and a distal end, the distal end having a cavity formed therein, and a advanceable tip housed within the cavity. The advanceable tip is advanceable to engage a surface of the target.

Abstract: A medical device is disclosed comprising an elongated needle assembly having a distal end, a proximal end and a longitudinal axis A, the needle assembly comprises a tubular cannula having a sharpened distal end, a proximal cannula portion, and a longitudinal bore along the longitudinal axis A,and a stylet configured to extend through the bore of the cannula,and having a blunt distal end and a proximal stylet portion. The needle assembly is provided with a spring member configured to urge the stylet in a distal direction along the longitudinal axis, such that the stylet is axially spring-biased in said distal direction.

Abstract: A collar for a surgical access device includes an annular body laterally attachable to a cannula of the surgical access device. A spring is coupled to the annular body and movable between an uncompressed state and a compressed state. The spring is configured to manipulate the annular body between a first condition and a second condition to selectively fix the annular body at predetermined locations along the cannula or to laterally remove the annular body from the cannula while the cannula is supported within a patient's body.

Abstract: A movement dampening system for a surgical tool. The system includes a height-adjustable base positionable adjacent to a surgical site on a patient. An elastic damper is disposed adjacent to the height-adjustable base, A channel extends through the elastic damper and the height-adjustable base to the surgical site. A portion of the channel extending through the elastic damper is sized to receive the surgical tool and to restrict movement of the surgical tool.

Abstract: An imaging needle apparatus includes a body, a needle coupled to the body, a probe, and an imager. The needle includes a needle body and a sharp tip. The probe can be exposed from the needle or housed within the needle body according to an operation being performed with the image needle apparatus. The imager is disposed inside of the probe, and includes a plurality of photocells.

Abstract: Needles are deployed in tissue under direct ultrasonic or other imaging. To aid in deploying the needle, a visual needle guide is projected on to the image prior to needle deployment. Once the needle guide is properly aligned, the needle can be deployed. After needle deployment, a safety boundary and treatment region are projected on to the screen. After confirming that the safety boundary and treatment regions are sufficient, the patient can be treated using the needle.

Abstract: A gripper head for grabbing and fixing a tick comprises two facing gripping jaws, wherein the gripper head can adopt a state with open gripping jaws and a state with closed gripping jaws. The gripper head further comprises a holder comprising a closing spring for holding the two gripping jaws, wherein the gripping jaws are configured such that each of them has a curved outer side and a flat inner side, the closing spring acts on the two gripping jaws, and in the closed state of the gripping jaws the flat inner sides of the two gripping jaws lie on each other such that a closed body is formed. The gripper head is design to be accommodated and fastened to a tick gripper.

Abstract: An external fixator system includes a proximal frame configured to restrict motion in a lower extremity of a subject, and a frame connector assembly. The proximal frame includes a first, second, and third component. The first component can support a first clamp to secure a first pin inserted within a bone extending between a foot and a knee of the lower extremity. The third component extends from a second end of the second component. The first, second and third components have longitudinal axes that are substantially coplanar. The third component includes an extension to extend over a dorsal portion of the foot of the subject and to support a second clamp to secure a second pin inserted within a bone of the foot. The frame connector assembly extends from the second component to support a third clamp to secure a third pin inserted within a third bone of the foot.

Abstract: A fastener device includes an anchor body that defines a through hole. The anchor body further includes an inner surface that defines a least a portion of the through hole. The fastener includes a head, a threaded shaft that extends out with respect to the head in a distal direction, and a neck between the head and threaded shaft. The head includes an outer surface configured to articulate along the inner surface when the fastener head is inserted in the through hole. At least a portion of the outer surface is convex and defines a portion of a sphere that defines a first diameter. The neck defines a second diameter and the fastener defines a ratio of the first diameter to the second diameter in a range between about 2 to 1 and about 3 to 1.

Abstract: Spinal fixation systems including a member, a first attachment portion, a second attachment portion, and an intermediate portion. The first attachment portion is attached at a superior end of the member and includes a first opening. The second attachment portion is attached at an inferior end of the member and includes a second opening. The intermediate portion connects the first and second attachment portions. The spinal fixation systems may also include a relief in at least one of the first opening and the second opening. The systems may also include a third attachment portion with a third opening and an intermediate portion with a first and a second elastic mechanism. The first elastic mechanism connects the first and third attachment portions and the second elastic mechanism connects the third and second attachment portions. Surgical methods for inserting the spinal fixation systems in a patient are also disclosed.

Abstract: Spinal fixation systems including a member, a first attachment portion, a second attachment portion, and an intermediate portion. The first attachment portion is attached at a superior end of the member and includes a first opening. The second attachment portion is attached at an inferior end of the member and includes a second opening. The intermediate portion connects the first and second attachment portions. The spinal fixation systems may also include a relief in at least one of the first opening and the second opening. The systems may also include a third attachment portion with a third opening and an intermediate portion with a first and a second elastic mechanism. The first elastic mechanism connects the first and third attachment portions and the second elastic mechanism connects the third and second attachment portions. Surgical methods for inserting the spinal fixation systems in a patient are also disclosed.

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

Abstract: A bone fastener comprises a first member defining an implant cavity and a groove configured for disposal of a band. The first member includes a part disposed with the implant cavity and engages with the band to provisionally fix the part relative to the first member. A second member is configured to penetrate tissue and includes a base that moves the part and engages the band to connect the members. Implants, systems, instruments and methods are disclosed.

Abstract: Embodiments herein are generally directed to spinal implants for use in orthopedic stabilization assemblies. In some embodiments, these implants may be used in conjunction with laminoplasty or laminectomy procedures.

Abstract: A spinal construct includes a fastener configured for attachment with sacral and/or pelvic tissue of a body. A connector includes a mating element engageable with the fastener and includes a receiver. A spinal implant is engageable with the receiver between a capture configuration and a removable configuration. A multi-axial fastener is connected with the spinal implant. Systems, implants, instruments and methods of use are disclosed.

Abstract: The present invention provides plate systems for distracting and fixating vertebral bodies of animal (preferably human) spines. In some embodiments, the system includes: a biocompatible plate with at least two holes, at least two biocompatible distraction screws for insertion through the holes, each screw having an expandable head, a bore and a threaded shank, and at least two biocompatible fixating screws with threaded shanks. Insertion of the fixating screws into the distraction screws causes the expandable heads to expand and lock to the biocompatible plate. Optionally, the plate and the expandable heads comprises mating teeth configured to lock the expandable heads to the plate upon expansion of the expandable heads. The present invention also relates to use of the plate system to distract and fixate vertebral bodies.

Abstract: An implant for osteosynthesis which can be used to repair fractures and or fuse joints. The implant comprises one or more through holes for the passage of one or more sutures therethrough and or one or more sutures may be an integral part of the implant. The one or more sutures may be used to pull bone segments together and create compression therebetween and or to affix soft tissue to a bone segment.

Abstract: A method and device for attaching a bone plate to a bone includes the steps of placing a first surface of a wire insertion device against the bone, inserting a reference wire through an opening of the wire insertion device extending therethrough from the first surface of the wire insertion device to a second surface of the wire insertion device, removing the wire insertion device from the reference wire and positioning a bone plate on the bone by moving the bone plate in a transverse direction relative to a longitudinal axis of the reference wire so that the reference wire is received within a slot of the bone plate, the bone plate including a first surface facing toward the bone and a second surface opposing the first surface, the slot open to a lateral side surface connecting edges of the first and second surfaces.

Abstract: According to one embodiment, a bone fixation system includes a plate having a first opening a beam configured to traverse through the first opening and reside proximate to a subchondral fragment of bone in an installed position. The beam may be operable to rotate about an axis of rotation proximate to the first opening and reposition the subchondral fragment of bone.

Abstract: An expandable screw includes generally a shaft, a head, and a cut pattern. The shaft includes a longitudinal axis, an outer surface including a thread to engage bone, and an expandable region configurable between a first state with a first radius measured from the longitudinal axis to the outer surface and a second state having a second radius measured from the longitudinal axis to the outer surface. The cut pattern on the shaft permits at least partial nesting of a first portion of the expandable region within a second portion of the expandable region in the second state. The central lumen is closed by the abutment of a top portion of the second cut surface with the bottom portion of the first cut surface so as to form a closed structure or fluid seal preventing a bone ingrowth inside the central lumen.

Abstract: A system for making a customized orthopedic surgical instrument for use in repairing a joint of a patient includes a computer system for generating computer-readable instructions to form a patient-specific orthopedic surgical instrument based at least in part on image data obtained from at least a portion of a bone corresponding to the joint of the patient; and a machine for forming a patient-specific orthopedic surgical instrument from the computer-readable instructions. The surgical instrument includes a resin composition including from about 50 wt % to about 90 wt % of a base thermoplastic and from about 10 wt % to about 50 wt % of a filler material. The base thermoplastic includes polyetherimide, polycarbonate, modified polyphenylene ether, polyamide, copolymers of these thermoplastics, and combinations thereof. The surgical instrument includes at least one surface portion having a shape that substantially conforms to a corresponding surface portion of the bone.

Abstract: A debris collection device includes first and second members that are moveable relative to each other between first and second configurations. In the second configuration, the first and second members interface with each other and define a restraint opening that is configured to receive an elongate element, such as a spinal rod. The first and second members while in the second configuration define a guide opening that intersects the restraint opening. Such guide opening is configured to receive a cutting tool, such as a conical burr, drill bit, mill or saw. The first and second members have walls that, when in the second configuration, collectively define an interior space that has a volume sufficient to collect debris created by cutting the elongate element through the guide opening. Methods of utilizing the debris collection device allow for cutting of a spinal rod or the like in situ while capture debris caused by the cutting procedure.

Abstract: A filtration system for use in connection with a central vacuum system in a hospital or other medical facility. In certain aspects, the filtration system comprises a removable filter for removing contaminants; a fitting adapted for connection to a central vacuum source/system which provides constant suction, which fitting is positioned between the filter and the central vacuum source; a flow control valve positioned between the filter and the fitting; wherein the relative positions of the fitting, flow valve and filter prevent contaminants from being discharged into the central vacuum system. In other aspects, the system provides variable filter life based upon variable flow.

Abstract: An electrosurgical snare device is provided which uses a flow of inert gas to assist in the cutting and sealing process of tissue, while substantially reducing the formation of eschar and collateral tissue damage. The electrosurgical device includes a housing having a longitudinal axis; a support shaft attached to a distal end of the housing, and an end effector coupled to a distal end of the support shaft. The end effector includes a tube including a plurality of apertures and an electrically conducting spring disposed around the tube, where a spacing of the coils of the spring coincides with a spacing of the plurality of apertures, wherein a gas assisted electrosurgical effect is formed at each of the plurality of apertures when an inert gas flows through the tube and the spring is energized. The tube may be configured as a loop or snare.

Abstract: A treatment device is disclosed, which includes a dissecting section main body which is configured to dissect tissue in a living body when inserted into the living body along a blood vessel, and which has a slit permitting a branch vessel branched from the blood vessel to enter into the slit, a stanching section which is disposed at the slit and which presses and cauterizes the branch vessel introduced into the slit, and a cutting section which is disposed at the slit and which cuts the cauterized branch vessel.

Abstract: A system and method can be used to denervate at least a portion of a bronchial tree. An energy emitter of an instrument is percutaneously delivered to a treatment site and outputs energy to damage nerve tissue of the bronchial tree. The denervation procedure can be performed without damaging non-targeted tissue. Minimally invasive methods can be used to open airways to improve lung function in subjects with COPD, asthma, or the like. Different sections of the bronchial tree can be denervated while leaving airways intact to reduce recovery times.

Abstract: A tissue treatment selection device that has at least one treatment delivery member, a delivery setting circuit that is coupled to the treatment delivery member that is adapted to be deployed into tissue to deliver therapeutic energy to a target tissue zone, and the processing circuit is operable to set treatment parameters in the delivery setting circuit that is operable to set treatment parameters in the delivery setting circuit. The processing circuit is operable to transmit a test signal through the deployed treatment delivery member and to determine deployment status. The treatment selection device has a processing circuit adapted to send a message to a display device that indicates that the deployed treatment delivery member has been determined to be compensable and contains a suggested change in the treatment parameters. Also presented herein is a method of treating a tissue of a patient using the treatment delivery device.

Abstract: A surgical instrument includes a first power source and a second power source. The first power source is configured to deliver power to a surgical instrument at a first rate of discharge. The second power source is configured to deliver power to the first power source at a second rate of discharge. The first power source and the second power source are positioned within the surgical instrument. The first power source and the second power source are further configured to communicate with a control module. The control module may rely on power from the first power source to drive an end effector of the surgical instrument. The end effector may comprise a harmonic/ultrasonic blade, RF electrosurgical electrodes, powered cutting/stapling features, and/or various other types of components.

Abstract: A system and method are provided for assessing the compliance of internal patient tissue for purposes of catheter guidance and/or ablation procedures. Specifically, the system/method provides for probing internal patient tissue in order to obtain force and/or tissue displacement measurements. These measurements are utilized to generate an indication of tissue elasticity. In one exemplary embodiment, the indication of elasticity is correlated with an image of the internal tissue area and an output of this image including elasticity indications is displayed for a user.

Abstract: An electrosurgical system includes an energy applicator adapted to direct energy to tissue, an electrosurgical power generating source, and a surface-contact detection device. The surface-contact detection device is operably associated with the energy applicator. The surface-contact detection device is communicatively-coupled to the electrosurgical power generating source. The surface-contact detection device includes at least one optical transmitter to generate optical signals, a lens member configured to reflect optical signals generated by the optical transmitter when the lens member is disposed in contact with tissue, and at least one optical receiver to receive optical signals reflected by the lens member. The electrosurgical power generating source is adapted to transmit energy to the energy applicator when it is determined that the lens member is disposed in contact with tissue.