Abstract: A method of inserting a woven retention device into a bone hole includes providing a woven retention device with a tapered distal end and a proximal end to receive a fastener, providing a delivery tube with distal and proximal openings, and providing a push rod to push the woven retention device through the distal opening of the delivery tube. The delivery tube includes a compression portion over at least a distal end of the delivery tube. The method also includes positioning the distal opening of the delivery tube near an opening of the bone hole and advancing the woven retention device through the compression portion of the distal opening of the delivery tube and into the bone hole by pushing on an interior of the tapered distal end of the woven retention device using the distal end of the push rod.

Abstract: A kit for implanting a woven retention device into bone includes a woven retention device, a delivery tube, and a push rod. The woven retention device includes a distal end that is tapered to a distal tip, a proximal end for receiving a fastener, and a sleeve body between the distal and proximal ends. The delivery tube includes distal and proximal openings, and a compression portion over at least a distal end of the delivery tube. The push rod can be slideably received within the delivery tube and has a distal end for pushing the woven retention device through the distal opening of the delivery tube.

Abstract: A method for fusing vertebral bodies comprising the steps of: mounting a first engagement member of a fixation member to a pedicle of a first vertebra and a second engagement member of the spinal fixation member to a pedicle of a second vertebra, the first engagement member having a first extension engaged with an expansion ring, the second engagement member having a second extension engaged with the expansion ring; inserting screws through the first and second engagement members and into the pedicles of the respective first and second vertebrae; rotating the expansion ring in a first direction, thereby distracting the first and second vertebrae; implanting an intervertebral implant between the first and second vertebrae after rotating the expansion ring in the first direction; and rotating the expansion ring in a second direction after implanting the intervertebral implant, thereby compressing the first and second vertebrae.

Abstract: Variations on improved pedicle screw coupling assemblies, along with methods for use of such assemblies provide improved functional characteristics over existing devices. A coupling assembly is capable of providing rigid fixed attachment between a pedicle screw fully seated to underlying bone and a member extending between adjacent pedicle screws. The coupling assembly includes a pedicle screw having a threaded shaft and a head portion. The head portion includes a driving feature and a proximally oriented bore having a bore diameter. In one version, the coupling assembly includes a member adapted to extend between adjacent pedicle screws. The member includes a protrusion adapted for insertion into the bore of the pedicle screw, the protrusion having a protrusion diameter that is larger than the bore of the pedicle screw head portion. In another version, the coupling assembly includes a spherical bore in the screw head.

Abstract: A pedicle screw implant construct kit, comprising at least one pedicle screw, at least one collar comprising a recess for receiving a rod, the collar configured to be coupled to a head of the pedicle screw, an elongated rod for connecting the collar to one more additional collars to couple between the pedicle screw and one or more additional screws, and a locking ring sized to be positioned over at least a distal portion of the collar to restrain relative movement of the screw head and rod by exerting radial compression force onto the collar. In some embodiments, the components of the kit are comprised of carbon reinforced composite material.

Abstract: Provided is a bi-dimensionally adjustable spacing device configured to be placed between the spinous processes of at least two adjacent vertebrae and also adjusted laterally to securely contact the lateral surfaces of the spinous process. A method of using the device to treat spinal disorders is also provided.

Abstract: A hinged bone screw and tool set is used for implanting such bone screws in a human spine, followed by the implantation of a longitudinal connecting member into the bone screws. The hinged bone screw includes a shank with an upper portion and a receiver with integral arms forming a U-shaped channel. A lower curved seat partially defining the U-shaped channel cooperates with an upper portion of the bone screw shank for hinged movement of the shank with respect to the receiver. The tool set includes an insertion tool, a bone screw driver, a reduction tool and a closure starter. The insertion tool includes a bone screw attachment structure and a laterally opening channel. The insertion tool further includes a threaded portion for cooperation with the reduction tool to provide synchronized placement of a closure structure in the bone screw receiver while reducing and capturing a longitudinal connecting member within the receiver.

Abstract: An assembly for surgically treating a chest-wall deformity may include an implantable stabilizer member, an implantable pectus bar and an implantable stopping member. The implantable stabilizer member may include first and second base parts and a channel defined by the first and second base parts. The stabilizer member may include first and second retaining bars extending between the first and second base parts and traversing the channel. The first and second base parts may be adapted to be secured to tissue of the chest wall. The implantable pectus bar may be receivable within the channel of the stabilizer member. The implantable stopping member may be adapted to be engaged with the pectus bar between the first and second retaining bars after the pectus bar is inserted into the channel to restrict movement of the pectus bar relative to the tissue.

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 application relates to a cross pin fixator device comprising a plate member with spherical cavities that are open to the front and to the back of the plate, collapsible pin holder members having a central channel for insertion of a bone pin, the collapsible pin holder member being press-fit into the spherical cavities, and bone pins individually inserted into the central channel of a pin holder. The application also relates to a method for treating a fracture of the proximal humerus using the proximal humerus cross pin fixator and to a kit for treating a fracture of a bone.

Abstract: The present invention relates to a bone plating system and method for fracture fixation of bone. The bone plating system includes a bone plate, at least one locking screw, and at least one non-locking screw. The bone plate has locking holes with threads and non-locking holes. The locking screws have a shaft with a thread for engaging bone and a head with a thread configured and dimensioned to mate with the thread of the locking holes. The non-locking screws have a thread for engaging bone and a non-threaded head. Both the locking and non-locking screws remain seated in their respective holes for substantially as long as the bone plate is implanted. The non-locking screws compress the bone plate against the bone and hold fracture reduction while the locking screws are secured to the plate at a fixed angular relationship. The mixed fixation achieved by this bone plating system and method is particularly useful for treatment of per-articular fractures.

Abstract: A bone fixation device is disclosed that permits some movement of different portions of a fractured bone when the device is affixed thereto. Various embodiments are disclosed, including bone plates that have fixed holes and floating holes therethrough for receiving bone screws, and bone plates including oblong holes allowing for screw movement.

Abstract: A method for locating a material having thermoplastic properties in pores of bone tissue includes providing a pin having the material having thermoplastic properties and a core, wherein the material having thermoplastic properties is arranged on the circumferential surface of the core constituting an outer region of the pin. An opening is provided in the bone tissue, and the pin is positioned at least partly in the opening. The outer region of the pin is then impinged with mechanical vibration energy for a time sufficient for liquefying at least part of the material having thermoplastic properties, and, in a liquefied state, pressing it into the pores of the bone tissue surrounding the opening. The vibration energy is stopped for a time sufficient for re-solidification of the liquefied material, and then the core is removed.

Abstract: A system for preparing and inserting a woven retention device into bone is provided. The system includes a woven retention device having a distal end, a proximal end for receiving a fastener, and a sleeve body between the distal and proximal ends. A longitudinal axis extends between the distal and proximal ends. The system also includes a measuring device surrounding at least a portion of the woven retention device and defining a cutting position at which the woven retention device is to be cut for insertion into a hole in the bone. The measuring device measures a distance from the distal end of the woven retention device to the cutting position. The woven retention device is movable relative to a least a portion of the measuring device that defines the cutting position such that the woven retention device can be cut to a desired size.

Abstract: A perforated sheath is anchored in a tissue opening with the aid of a tool, wherein the anchorage is achieved with the aid of mechanical vibration and a material which is liquefiable by the vibration. The tool includes a vibrating element and a counter element. Distal portions of both elements are introduced into the sheath to be in contact with each other at an interface. The vibrating element is connected to a vibration source and the vibrating element and the counter element are held against each other for effecting liquefaction of the liquefiable material at the interface. Under the effect of the force applied to the vibrating and counter element for holding them against each other, the liquefied material flows from the interface through the sheath perforation and penetrates the tissue.

Abstract: An expandable implant includes an implant body defining an internal void, the implant body including a plurality of interconnected linkages. A first plurality of the linkages has an expansion characteristic that is different from a second plurality of the linkages. An expandable bladder is sized to be disposed in the internal void. The bladder defines a bore configured to receive an expansion material, such that the expansion material applies an expansion force against the bladder, which thereby applies the expansion force against the implant body so as to cause the first linkage to expand greater than the second linkage. The expandable implant can be placed in a fracture location so as to restore height to a fractured target bone.

Abstract: An alignment tool (2) for a joint is provided comprising a reference member 4 that defines a reference plane R and a distraction member (6). The distraction member (6) comprises first and second distraction arms (70, 72), each of which is independently moveable with respect to the reference member (4) along a movement axis M. The movement axes M, M of the first and second distraction arms (70, 72) are substantially parallel. A kit of parts is also provided comprising an alignment tool (2), a drill guide (200) and a cutting guide (300).

Abstract: A implanting device for driving a fastener or fixation element into bone is described. Also described are methods for using a implanting device for driving a fastener or fixation element into bone and a kit comprising a pneumatic implanting device for driving a fastener or fixation element into bone.

Abstract: An adapter for putting two incompatible medical systems in fluid communication with each other. The adapter may have a continuous outer diameter and may include two segments: a first segment composed of a rigid material and including a first portion and a second portion, the first portion having a continuous outer diameter and the second portion defining one or more flanges, the first segment defining a first passage therethrough; and a second segment composed of a flexible material and coupled to the first segment, including a first portion and a second portion. The first portion of the second segment may have an inner surface configured to surround the flanges of the second portion of the first segment, and the second portion of the second segment having a tapered inner surface, the second segment defining a second passage therethrough that is continuous with the first passage.

Abstract: A device, system, and method for enhancing cooling uniformity and efficiency of cryogenic fluids and providing a treatment element the shape of which can be adjusted for multiple purposes. The device may include a balloon catheter and fluid dispersion element, the fluid dispersion element directing the flow of coolant from a fluid injection element the interior wall of the balloon. The method of changing the shape of the treatment element may include retracting and extending a shaft to which the distal neck of a balloon is coupled, so that the balloon goes from a first shape to a second shape.

Abstract: A method of controlling RF power delivered from a bipolar electrosurgical instrument into a biological tissue. The method comprises controlling the profile of a RF waveform by: setting a maximum voltage limit for a voltage applied across the bipolar electrosurgical instrument; calculating a tissue resistance, the calculating step including a correction for an impedance associated with the RF channel; determining an objective tissue current limit from the calculated tissue resistance and a predetermined power dissipation target; and dynamically adjusting the current limit based on the determined objective tissue current limit. This control method may ameliorate the impact of an increased cable length on the accuracy of control of RF waveforms delivered to the tip of the probe.

Abstract: An electrosurgical system is provided. The electrosurgical system includes an electrosurgical generator including a computer having one or more microprocessors in operable communication with memory for storing information pertaining to the electrosurgical generator. An audio output module is in operable communication with the computer and configured to generate an audio output having the information pertaining to the electrosurgical generator embedded therein. A speaker is in operable communication with the audio output module for outputting the audio output. A recording device is configured to record the audio output. An audio collector is configured to receive the audio output from the recording device and decipher the embedded audio so that the information pertaining to the electrosurgical generator may be utilized for future use.

Abstract: A treatment system comprises a first power supply apparatus and a second power supply apparatus each connectable with a surgical device and a neutral electrode, the first power supply apparatus being electrically connected with the second power supply apparatus, the treatment system treating a living tissue while performing transmission and reception of information between the first and second power supply apparatuses, wherein, in a case where the neutral electrode is connected to only one of the first and second power supply apparatuses, an output of the surgical device connected to the second power supply apparatus is inhibited during an output of the surgical device connected to the first power supply apparatus, and the output of the surgical device connected to the first power supply apparatus is inhibited during the output of the surgical device connected to the second power supply apparatus.

Abstract: A coating system comprising at least one layer made at least essentially of ZrO2 which is used for providing insulating properties to parts of medical devices, particularly of electrosurgical devices.

Abstract: Surgical instruments and methods for controlling temperature are described herein and can have particular utility when sealing tissue. In one embodiment, an end effector can include first and second jaw members configured to clamp tissue therebetween, and an electrode having a single continuous conductive surface that is coupled to the first jaw member. The end effector can also include a plurality of electrical insulators of varying thermal conductivity disposed between the electrode and the first jaw member coupled thereto. The electrode can be divided into a plurality of thermal zones by at least one opening formed therein and the plurality of electrical insulators can be arranged such that at least a first thermal zone contacts an electrical insulator having a first thermal conductivity and at least a second thermal zone contacts an electrical insulator having a second thermal conductivity that is higher than the first thermal conductivity.

Abstract: A method of transferring a battery assembly to a battery-powered surgical instrument includes releasably engaging a battery jacket with the battery assembly, transferring the battery jacket, having the battery assembly engaged thereto, to a battery-powered surgical instrument, and releasably engaging the battery jacket with a handle of the battery-powered surgical instrument such that the battery assembly is electrically coupled to the battery-powered surgical instrument and such that the battery jacket and the handle cooperate to enclose the battery assembly therein. Aseptic battery jackets for such use are also provided.

Abstract: An electrosurgical instrument includes a housing, a shaft extending from the housing, and an end effector assembly attached at a distal end of the shaft. A handle assembly is coupled to the housing and includes a movable handle for manipulating the end effector assembly. An outer sleeve is disposed about the shaft and selectively translatable relative thereto. An energizable member is operably coupled to the outer sleeve. A deployment mechanism is provided including a lever rotatably coupled to the housing and positioned proximally of the movable handle and at least one link member coupled between the lever and the outer sleeve. The link member(s) couple to the outer sleeve distally of the movable handle. Rotation of the lever translates the outer sleeve distally to move the outer sleeve over the end effector assembly and simultaneously deploy the energizable member distally past the end effector assembly.

Abstract: A surgical instrument includes a housing, an inner shaft coupled to and extending distally from the housing, an end effector assembly disposed at a distal end of the inner shaft, an outer sheath that is fixed to the housing, extends distally from the housing, and is disposed about the inner shaft, and an insulative sleeve. The insulative sleeve is positioned between the inner shaft and the outer sheath. The insulative sleeve is movable relative to the inner shaft and the outer sheath between a storage position, wherein the insulative sleeve is positioned proximally of the end effector assembly, and a deployed position, wherein the insulative sleeve substantially surrounds the end effector assembly.

Abstract: A method of forming a jaw member of an end effector includes providing a metal support base; engaging a plurality of ceramic stops to the metal support base; and coupling an insulative plate and a sealing plate to the metal support base by aligning the plurality of ceramic stops through a plurality of openings defined in the insulative plate and a plurality of openings defined in the sealing plate.

Abstract: A surgical instrument includes a housing, an energizable member selectively deployable relative to the housing, and a deployment mechanism. The deployment mechanism includes a fixed gear rotatable in opposite directions to move the energizable member between the deployed and storage positions. The deployment mechanism further includes an actuator assembly having a first actuator and a first gear, and a reversing assembly. The actuator assembly is movable relative to the fixed gear between an engaged position and a spaced-apart position. The reversing assembly includes a second actuator and a second gear that is movable between a removed position, wherein the first gear is disposed in the engaged position and the second gear is disengaged from the first gear and the fixed gear, and an inserted position, wherein the first gear is moved to the spaced-apart position and the second gear is engaged between the first gear and the fixed gear.

Abstract: A surgical instrument includes a housing, a rotating assembly including a rotation wheel coupled to the housing, a shaft engaged with the rotation wheel within the housing and extending distally from the housing, an end effector assembly disposed at a distal end of the shaft, a drive assembly slidably disposed within the shaft and operably coupled to the end effector assembly for manipulating the end effector assembly, a knife assembly slidably disposed within the shaft translatable relative to the end effector assembly between a retracted position and an extended position, an elongated insulative sheath slidably disposed about the shaft, and an energizable member slidably disposed within the shaft. The instrument is configured such that rotation of the rotation wheel relative to the housing similarly rotates the shaft, end effector assembly, drive assembly, knife assembly, elongated insulative sheath, and energizable member relative to the housing.

Abstract: A surgical instrument includes a housing having a shaft extending distally therefrom, an end effector assembly disposed at a distal end of the shaft, a handle assembly coupled to the housing for manipulating the end effector assembly, a deployable assembly, at least one actuator for deploying and retracting the deployable assembly, and a closure member. The closure member is keyed to the actuator(s) and operably positioned relative to the movable handle of the handle assembly such that, upon rotation of the actuator(s) relative to the housing from an un-actuated position to an actuated position, the closure member is urged into contact with the movable handle to urge the movable handle from an initial position to a compressed position, thereby moving the end effector assembly to an approximated position.

Abstract: A surgical instrument includes a housing having a shaft affixed thereto, a reciprocatable drive rod slideably disposed at least partially within the shaft, and a force applicator coupled to the drive rod. The shaft includes first and second jaw members attached to a distal end thereof, at least one of which movable relative to the other from a first position wherein the jaw members are disposed in spaced relation relative to one another to at least a second position closer to one another wherein the jaw members cooperate to grasp tissue therebetween. The force applicator and the drive rod mechanically communicate to impart movement to at least one of the jaw members. The bipolar forceps includes a handle assembly and a force-balance interface. The force-balance interface configured to translate a multiple of the user-applied force exerted on the handle assembly into the jaw members.

Abstract: An endoscopic bipolar forceps includes a housing and a shaft, the shaft having an end effector assembly at its distal end. The end effector assembly includes two jaw members for grasping tissue therebetween. The jaw members are adapted to connect to an electrosurgical energy source which enable them to conduct energy through the tissue to create a tissue seal. A drive assembly is disposed within the housing which moves the jaw members. A switch is disposed within the housing which activates the electrosurgical energy. A knife assembly is included which is advanceable to cut tissue held between the jaw members. A movable handle is connected to the housing. Continual actuation of the movable handle engages the drive assembly to move the jaw members, engages the switch to activate the electrosurgical energy source to seal the tissue, and advances the knife assembly the cut the tissue disposed between the jaw members.

Abstract: A surgical instrument includes a housing, an energizable member, and a deployment mechanism. The deployment mechanism includes a one-way rotatable member, a linkage, and an actuator. The first end of the linkage is coupled to the one-way rotatable member at an offset position. The second end of the linkage is coupled to the energizable member such that a revolution of the one-way rotatable member moves the energizable member from the storage position to the deployed condition and back to the storage position. The actuator is selectively actuatable from an un-actuated state to an actuated state. Each actuation of the actuator effects a partial revolution of the one-way rotatable member such that each actuation of the actuator moves the energizable member from one of the storage position or the retracted position to the other of the storage position or the retracted positions.

Abstract: A surgical instrument includes a housing, an energizable member, and a deployment mechanism. The energizable member is movable relative to the housing between a storage position and a deployed position. The deployment mechanism includes a first actuator member movable relative to the housing from a first un-actuated position to a first actuated position to move the energizable member from the storage position to the deployed position and a second actuator member movable relative to the housing from a second un-actuated position to a second actuated position to move the energizable member from the deployed position to the storage position. Movement of the first actuator member from the first un-actuated position to the first actuated position effects movement of the second actuator member from the second actuated position to the second un-actuated position and vice versa.

Abstract: A deployment and retraction mechanism for a surgical instrument includes a gear box defining a longitudinal slot, a slider, a ring gear, and a planet gear. The slider is configured to engage a deployable component of the surgical instrument and is translatable along the longitudinal slot between a proximal end, corresponding to a storage condition of the deployable component, and a distal end, corresponding to a use condition of the deployable component. The planet gear is operably engaged with the ring gear and configured to orbit within the ring gear. The planet gear includes an off-center pin rotatably supporting the slider thereon. The planet gear and ring gear are configured such that a one-half orbit of the planet gear within the ring gear translates the slider from one end of the longitudinal slot to the other end of the longitudinal slot.

Abstract: A surgical instrument for supplying energy to tissue can comprise a jaw member comprising an electrode, wherein the electrode is configured to supply energy from a power source to captured tissue. The surgical instrument comprises a tissue-cutting element to transect the captured tissue. The rate of distal translation of the tissue-cutting element during the operational stroke may be regulated by a damper. The damper may have barrel and a plunger.

Abstract: A family of barrel structures is provided in a kit. Each barrel structure is differently sized and configured for advancement into anal canals of different anatomic morphologies. Instructions are provided for using the barrel structures to treat an individual. The instructions instruct assessing an anatomic morphology of an anal canal of an individual to be treated and selecting one of the barrel structures based upon the assessed anatomic morphology. Each barrel structure carries an electrode sized and configured to be coupled to a source of tissue ablation energy to be applied through the electrode to form a lesion. Each barrel structure includes a transparent side wall visualized by a direct line of sight from an end portion of the first barrel structure. The instructions instruct inserting the selected barrel structure into the anal canal and visualizing by the direct line of sight through the transparent side wall of the selected barrel structure the dentate line and the targeted tissue region.

Abstract: Provided herein are methods, systems, and devices for increasing heat shock protein expression and treating conditions for which increased heat shock protein expression is expected to be beneficial using thermal ablation.

Abstract: A steerable catheter system is provided including an elongated shaft having a proximal end, a distal end and an outer surface. The outer surface includes at least one cavity configured to facilitate movement of the distal end relative to the proximal end so as to steer the elongated shaft. A catheter tip is attached to the distal end of the shaft. The catheter tip comprises a curved body having at least one RF cutting edge and at least one non-cutting area recessed from the at least one cutting edge.

Abstract: An ablation device for denervation including a catheter delivery mechanism including an elongated tube with a distal end and a proximal end, the distal end being emplaceable within a body lumen at a target nerve region. A guide wire, at least one radiofrequency electrode, a plurality of positioning elements, and a plurality of pressing elements initially located within the tube. The electrode being deployable from the tube at the target nerve region and forming a ring-shaped structure adjacent the distal tube end. The positioning elements being deployable from the tube at the target nerve region from a position of the tube further distal than the electrode. The pressing elements being deployable from the tube more proximal than the electrode for use in pressing the deployed electrode against tissue to be ablated.

Abstract: The present invention relates to a method of removing a tumor by radiofrequency ablation, comprising providing a guiding device (6) having at least two first concentric through holes (8, 81, 82) and a plurality of second through holes (10, 11) at a periphery of the guiding device (6). The method further comprising placing the guiding device against the skin of a patient and inserting two first electrodes (3, 4, 5) into the first through holes (8, 81, 82) of the guiding device and into a patient's skin and then applying a first radiofrequency current between the two first electrodes (3, 4, 5). The method further comprising inserting a second electrode (5) through a second through hole (10, 11) and into the patient's skin and then applying a second radiofrequency current between a first electrode (3, 4) and the second electrode (5).

Abstract: A method for treating Chronic Obstructive Pulmonary Disease (COPD) or chronic bronchitis to alleviate the discomforts of breathing by using non-thermal electroporation energy to ablate diseased portions of the lung including the bronchus, airways and alveoli which, in effect, opens the restrictive diseased portions thereby maximizing the overall surface area thereof causing improved airflow and uninhibited breathing.

Abstract: A microwave providing device is provided, which is capable of effectively extending the coagulation range of a treatment target tissue by setting the conditions for intermittently providing microwaves. An output controller controls a microwave generator based on a first efficiency of dielectric heating by microwaves with respect to a cumulative radiation period of microwaves radiated intermittently to a treatment target tissue S and a second efficiency of dielectric heating by microwaves with respect to a cumulative radiation period of microwaves radiated continuously to the treatment target tissue so that microwaves are intermittently radiated at least after a reference cumulative radiation period that is set in advance as a cumulative radiation period at which the first efficiency becomes larger than the second efficiency.

Abstract: The invention provides a non-invasive device (100) for treatment of skin tissue using laser light, and it provides a method and a computer program product. The non-invasive device comprises a light emission system (110) for generating a first laser pulse (130) and a subsequent second laser pulse (150) at a predefined time delay (?T) after the first laser pulse. The non-invasive device further comprises an optical system (160) for focusing, in use, the first laser pulse and the second laser pulse at a treatment location (210) inside the skin tissue (200). The first laser pulse comprises a first power density, a first pulse duration and a first pulse energy for initiating a plasma (205) at the treatment location.

Abstract: A medical device used in a medical robotic system has a conduit and an orientable tip. An optical fiber coupled to a laser source and/or a catheter coupled to one or more biomaterial sources extends through the conduit and tip so that the tip of the medical device may be robotically directed towards a target tissue for laser and/or biomaterial application as part of a medical procedure performed at a surgical site within a patient. A protective sheath covers the fiber as it extends through the conduit and tip. A first coupler adjustably secures at least the sheath to the medical device and a second coupler adjustably secures the fiber to at least the sheath. A similar dual coupler mechanism may be used to secure the sheathed catheter to the medical device.

Abstract: A package for an orthopedic device is disclosed. The package includes inner and outer packaging and preferably allows for accessibility of the orthopedic device without direct handling by hand. Methods of utilizing such packaging are also disclosed.

Abstract: Devices and systems can be configured to guide an instrument to a target region. The guide system may include an imaging guide including a first segment, the first segment including a guide region and imaging coils surrounding the guide region; and a platform. The platform may include a first rail, a second rail disposed parallel to the first rail, and a positioning member disposed between the first rail and the second rail. The positioning member may include a positioning frame having an entry region. The positioning frame may be movably disposed with respect to the first and second rails in a first direction and a second direction that is perpendicular to the first direction. The platform may be disposed with respect to the imaging guide so that a position of the entry region is within the guide region.

Abstract: The various embodiments disclosed herein relate to arms or forearms of medical devices that are configured to couple with quick-release end effectors, quick-release end effectors for use with such medical devices, and arms or forearms coupled to such quick-release end effectors. Certain forearms and end effectors have magnetic couplings, while others have mechanical couplings, and further implementations have both magnetic and mechanical couplings.