Abstract: The invention being disclosed describes a medical device for removal of a thrombus or clot in a vascular setting by using a rotational, expandable basket structure in combination with drug infusion, blood/particle aspiration and clot isolation by distal and proximal occlusion.

Abstract: A medical assistance device is provided for insertion of a needle-like instrument. The device comprises a guide unit, a mechanism including the guide unit, a driving source configured to drive the mechanism, a needle sensor; and an anti-driving unit. The medical assistance device can detect the insertion state of a needle-like device and, when required, the anti-driving unit prevents operation of the driving source.

Abstract: A combined imaging probe holder and interventional needle guide assembly is provided. The imaging probe holder supports an imaging device (e.g., ultrasound probe) in a known relationship with a biopsy/treatment device holder such that a delivery element or interventional needle is constrained within an imaging field of the imaging device. Constraining the biopsy treatment device within the imaging field allows for real-time monitoring of the biopsy/treatment device during insertion of the interventional needle into patient tissue. In addition, the biopsy/treatment device holder is angularly positionable relative to the image field to allow advancement of the delivery element to any desired location within the imaging field.

Abstract: A steering adjustment for a needle visualization ultrasound system includes a needle, an ultrasound interface and one or more processing electronics. The ultrasound interface receives ultrasound imaging information from a first set of ultrasound firings. The processing electronics are coupled to the ultrasound interface. The processing electronics utilize the information from the first set of firings and identify the angle of the needle and the optimized steering frame angle. The processing electronics are further configured to cause a second set of firings. The second set of firings are configured for the identified needle angle and steering frame angle. The processing electronics are further configured to utilize the ultrasound information from the second set of firings to adaptively and dynamically enhance the visualization of the needle.

Abstract: Survival of patients suffering from many infections diarrheal diseases, including Ebola, as well as trauma and post-partum hemorrhage is improved with large-volume, parenteral, fluid replacement. In lieu of IVs, Intra-Osseous (IO) lines are placed with the help of a Humerus-Finder™, a one-piece guide that identifies the humeral head at the shoulder and allows for easy, safe, placement of an IO line. This guide enables healthcare providers and lay-providers to place IO lines and deliver fluids to infected persons without direct contact, limiting risk to providers. The Humerus-Finder™ makes early, potentially life-saving, supportive treatment available where large-volume fluid infusion can save lives and is useful in disaster medicine and emergency medicine when it is not possible to place an IV line rapidly and safely by helping first responders achieve IO access for delivery of fluid resuscitation in a safe, reliable manner.

Abstract: A guidance system for assisting with the insertion of a needle into a patient body is disclosed. The guidance system utilizes ultrasound imaging or other suitable imaging technology. In one embodiment, the guidance system comprises an imaging device including a probe for producing an image of an internal body portion target, such as a vessel. One or more sensors are included with the probe. The sensors sense a detectable characteristic related to the needle, such as a magnetic field of a magnet included with the needle. The system includes a processor that uses data relating to the sensed characteristic to determine a 3-D position of the needle. The system includes a display for depicting the position of the needle. The needle can include a donut-shaped magnet disposed about the needle cannula, or a removable stylet with a magnetic element and a strain gauge for detection of the needle distal tip.

Abstract: A medical device includes an elongated body (14) and a plurality of sensors (10) conformally formed on the elongated body at a plurality of longitudinal positions along the elongated body. The plurality of sensors is configured to generate signals in accordance with detected energy for an imaging system. A single electrical trace (24) connects to each of the plurality of sensors, the plurality of sensors being connected in parallel to form an array of sensors along the elongated body.

Abstract: A subintimal recanalization catheter, including an elongate shaft including a first tubular member and a penetration member slidably disposed in a lumen of the first tubular member. The penetration member includes a distal tip positioned proximal of a distal nose of the first tubular member. The distal nose of the first tubular member includes a ramp and a guide wire lumen extending through the distal nose of the first tubular member. Longitudinal movement of the penetration member relative to the first tubular member causes the penetration member to contact the ramp to direct the distal tip of the penetration member away from the first tubular member.

Abstract: Provided is a manual follicle-transplanting hair transplanter for increasing a graft survival rate. The manual follicle-transplanting hair transplanter includes a needle member having a lower end containing a follicle to be transplanted and having a head having a larger diameter than a portion below the head at an upper end thereof, a rod member inserted into the needle member and having a push portion having a larger diameter than a portion below the push portion at an upper end thereof, an inner body configured to contain the needle member and limit downward movement of the needle member, and an outer body configured to contain the inner body and limit upward movement of the needle member. The needle member is automatically withdrawn when a compressed spring disposed in the inner body expands and pushes up a lower surface of the head.

Abstract: Provided is an automatic hair transplanter for transplanting follicles including a housing having a space therein and having a nozzle in which an opening is formed on a front surface, a needle supply magazine installed on the housing and sequentially supplying a plurality of needles containing follicles to the back of the nozzle, a needle aligner transferring and aligning a needle supplied from the needle supply magazine with the center of the nozzle, a needle actuator causing the needle aligned by the needle aligner to protrude from the nozzle, a follicle pressurizer pressurizing a follicle in the needle protruding by the needle actuator from the back to the front, a needle retrieval magazine containing the needle in which pressurization of the follicle has been finished by the follicle pressurizer and nothing remains, and a manipulator having a switch for controlling operation of the needle actuator and the follicle pressurizer.

Abstract: Provided is an automatic hair transplanter for transplanting follicles including a housing having a space therein and having an aperture in a front surface, a cartridge installed behind the aperture and having a plurality of holes containing each of needle and rod assemblies, a cartridge driver configured to sequentially cause centers of the needle and rod assemblies to correspond to the center of the aperture by causing the cartridge to make a rectilinear motion or a rotary motion, a needle-and-rod assembly pressurizer configured to pressurize the back end of a needle and rod assembly whose center corresponds to the center of the aperture, and a manipulator having a switch for controlling operations of the cartridge mover and the needle-and-rod assembly pressurizer.

Abstract: A pair of cooperating catheters are used together to provide rapid access to the Left heart for diagnostic or therapeutic interventions. The initial entry point for the catheter pair is the groin. The pair of catheters can be used to carry out an electrographic determination of the location of the Fossa Ovalis on the septum. Features on the Catheter system permit quick and reliable confirmation of the catheter location via echo or x-rays. Once across the septum the inner catheter is removed from the outer catheter and a standard intervention may be carried out through the lumen of the outer catheter.

Abstract: A surgical device for treating shoulder dystocia having a first arm having a proximal portion, a distal portion and a first curved surface, a second arm having a proximal portion, a distal portion and a second curved surface and a shoulder engagement section positioned at least between the distal portion of the first and second arms and connecting the first and second arms. The engagement section has an atraumatic surface and is configured to contact and press down on the baby to reposition the baby upon manipulation of the first and second arms.

Abstract: A bone securement apparatus includes a bone plate configured and dimensioned to be applied across a joint of at least two bones or a space between at least two bone fragments. The bone plate includes first and second openings. A beaming member is configured to pass through the first opening, and the beaming member includes a third opening. A support member is configured to pass through the second opening and the third opening.

Abstract: An intervertebral spacer for therapeutic treatment of a patient includes a link sized and dimensioned to fit within an intervertebral space in the patient, and is configured to maintain a separation of two adjacent vertebrae for a period of time. A rigid guiding object, which may be a tool or a successive link, is insertable into the patient, to guide the link into the patient using an MIS approach. A pivot is connected within the links configured to limit a relative range of angular orientation between the link and the guiding tool.

Abstract: Medical implants and implant components are formed by additive manufacturing processes. The additive manufacturing process used results in the implants or implant components having surfaces having a higher coefficient of friction as opposed to a similar implant manufactured using a different process, such as having a machined surface. The higher coefficient of friction of the relevant surface is particularly useful for multi-component implants that are to have a fixed relationship between the components based at least in part on a frictional engagement between them. While manufacturing via an additive manufacturing process may result in an implant component having slightly less strength for its size when compared with traditional manufacturing methods, the advantage of the increased coefficient of friction may offset any loss of component strength, and may allow for overall reduced implant size while maintaining other desirable implant characteristics.

Abstract: A bone fixation element includes a distal end defining a longitudinal axis and being configured to penetrate tissue, a proximal end defining an axial opening disposed in communication with a transverse passageway and a fastener including a proximal portion having spaced apart walls that define an implant cavity and a distal portion disposed with the transverse passageway and configured to penetrate tissue. The distal end is disposable in spaced apart relation to the distal portion of the fastener within tissue. Methods of use are disclosed.

Abstract: A pedicle screw assembly has a bone screw, a tulip, a multi-segmented locking member and a saddle. The multi-segmented locking member is internal of the tulip positioned in a recess or undercut groove of an inner surface of the tulip. The saddle has a proximal end for engaging a rod and a distal end for receiving a head of the bone screw. The saddle has an exterior surface positioned between the ends. The outer surface is sized to move axially inside the tulip.

Abstract: A bone anchoring device includes a receiving part with a rod receiving portion having a first end, a second end, a recess for the rod, an outer surface, and a first engagement structure on the outer surface that extends farther radially outwardly than other parts of the rod receiving portion, and a flexible head receiving portion for inserting and clamping the head. The bone anchoring device also includes a locking ring configured to be arranged around the head receiving portion for locking the head, the locking ring having an outer surface and a second engagement structure on the outer surface that extends farther radially outwardly than the outer surface of the rod receiving portion. The engagement structures are configured to be engaged by an instrument to move the locking ring from a locking position to a position where the inserted head is pivotable.

Abstract: An implant having a receiver that is adapted to receive a polyaxial screw in the bore and either an internal or external cap. The cap can be an external or internal cap and the implant further has at least one locking aid in the form of at least one of a tactile feedback, a visual feedback or an enhanced fixation between the cap and a rod that is received in the receiver.

Abstract: A device is for fixing surgical implants in place. The device may include a central body having an axially hollow upper zone, and an axially hollow lower zone. The upper and lower zones may form a single body being open at the bottom and at the top. A central through cavity may extend inside the upper and lower zones. The upper zone may have two portions projecting axially from the upper zone, divided from each other by two through U-shaped slots and forming, in conjunction with part of the central cavity, a channel for housing a connection rod. The lower zone may include a slot for the lateral access to the central cavity of an anchoring device. The slot may be in a conformation such as to permit the lateral insertion of the anchoring device inside the central cavity.

Abstract: Described herein is an orthopedic fixation device for use in spinal surgery. Said orthopedic device is a pivoting device that comprises one or more hinges. Fixation of multiple vertebrae is accomplished by fixation at the vertebral facet joints. Multiple device may be further fixed at multiple vertebral levels with the use of a multi-level rod.

Abstract: This equipment comprises an iliac rod (2), a connection assembly (3, 4) for connecting that iliac rod to a vertebral bar, an iliac anchoring member and an iliac part connecting the iliac rod to that iliac anchoring member; said connecting assembly (3, 4) is independent of the iliac rod (2) and comprises two portions, namely: —a first portion (3), for connecting to said vertebral bar (50), that forms a closed conduit (10) for engagement of that portion (3) on that bar (50); and —a second portion (4), for connecting to said iliac rod (2), that forms a conduit (12) for the engagement of that second portion (4) on the iliac rod (2).

Abstract: A bone plate system is provided. The system includes two or more fastener locks stacked on top of each other and located between two holes in a plate adapted to receive bone fasteners. An actuator is provided between the locks. As the actuator is advanced, the locks are moved sequentially into position, firstly, to prevent one or more bone fasteners from backing out of the plate while permitting the fasteners to angulate and, secondly, to lock the angulation of the bone fasteners while still providing back out protection in situ. An expandable bone plate having a top plate interconnected to a bottom plate by a rack and pinion is provided. The rotation of the pinion with a driver lengthens or shortens the plate incrementally for custom length adjustment. The length is fixed in position with the simple removal of the driver and no further step is required to lock the plate length.

Abstract: Devices and methods for treating degenerative conditions of the spine or for alleviating pain or discomfort associated with the spinal column are disclosed. In particular, laminoplasty fixation devices and methods are disclosed. Also disclosed, is a vertebral implant comprising a first bone engaging portion configured for securing to a first cut portion of a vertebra and a second bone engaging portion configured for securing to a second cut portion of the vertebra. A body portion is provided for associating the first and second bone engaging portions at a preselected spacing from each other, wherein the implant is adjustable to select said spacing.

Abstract: A facet joint replacement system includes an inferior implant with an inferior articular surface, a superior implant with a superior articular surface, and an optional crossbar. The inferior implant and the superior implant are each polyaxially adjustably connected to fixation elements which anchor the implants to adjacent vertebrae. The optional crossbar may be polyaxially adjustably connected to bilateral implants. The system components may be provided in kits which provide components of various sizes and shapes. A set of surgical instruments may facilitate implantation of the facet joint replacement system by providing tools for bone preparation, trialing, implant insertion, implant alignment, and lock-out of modular interconnections.

Abstract: A device for placement between two adjacent spinous processes of a spinal column to treat a spinal condition, and a method for performing a procedure on a spine of a patient, are provided. The device may include a first member, a second member mounted onto the first member, and a locking plug configured to restrict movement of the second member relative to the first member. The method may include positioning a portion of a first member between two adjacent spinous processes of the spine, advancing a second member along a length of the first member, and restricting the second member from moving relative to the first member.

Abstract: A surgery device assembly for minimally invasive spinal surgery is provided. The surgery device assembly includes a plurality of pedicle screws, a least one parallel bridge, a guiding device and an elongated rod. The plurality of pedicle screws are drilled into the corresponding spine respectively. Each pedicle screw is clamped by the corresponding parallel bridge in order to keep the cannulas parallel to each other. The top of the sidewalls is a U-type trough in order to adjust a direction of each pedicle screw to the same way. The proper shape of the elongated rod is bent according to the curve formed with the U-type grooves of pedicle screws. The elongated rod is seated in trough portion of each pedicle screw by puncturing the guiding device. The elongated rod is then secured by nuts in order to fix a bony structure.

Abstract: Rod delivery tools, methods for delivering a connecting rod of a pedicle screw system into seating slots of at least first and second long arm screw towers of a pedicle screw system, and a rod reduction tool and related methods for urging a distal leading end of a connecting rod and an opening of a long arm screw tower into alignment with one another, where the two are initially misaligned.

Abstract: Implantable devices for fixation of curved bone such as the pelvic ring pubic symphysis and acetabulum, and methods for the use of the devices are disclosed. The implantable devices are convertible between a flexible state and a rigid state, and include an elongate structure having a proximal bone interface, a main body, and a distal bone interface. In a flexible state, the devices may be inserted along, and conform to a curved pathway, and in the rigid state, the devices may support the mechanical loads required to fixate a fracture.

Abstract: Apparatus for treating a bone fracture, the apparatus comprising: an anchoring tube comprising a hollow elongated shaft adapted for disposition in a hole formed in a bone and having a distal end, a proximal end and a lumen extending therebetween, and a substantially planar plate mounted to the proximal end of the hollow elongated shaft and adapted for disposition against the outer surface of the bone; wherein the plate comprises a top surface and a bottom surface, and further wherein the bottom surface of the plate is convex, such that when the anchoring tube is disposed in a hole formed in a bone and is rotated about the longitudinal axis of the hollow elongated shaft, the convex bottom surface of the plate maintains supporting contact with the outer surface of the bone.

Abstract: Systems for trauma and/or joint fusion implants and instruments include transarticular screw and intra-articular washer, polyaxial screw and plate, single- and multi-level polyaxial bone clamps, and minimally invasive adaptations.

Abstract: A cervical plate having improved mounting screws that employ a retention clip for automatically engaging the head portion of the screw during insertion into countersunk apertures. The arrangement prevents the mounting screws from migrating out of the bone material during use.

Abstract: The present disclosure relates to an interference screw having a body with a proximal end, distal end, and longitudinal axis extending between thereinbetween. The screw further includes threads for fixing the screw into bone. The screw further includes a through bore defined by the body. The through bore extends between the proximal and distal ends along the longitudinal axis, and has a surface. The screw further includes a controlling member formed by the through bore surface. To install the screw into bone, a surgeon turns the screw with a driver that engages with the controlling member. The driver only engages the controlling member when it is in a driving orientation with respect to the controlling member. Advantageously, with this “one-way” engagement the surgeon can control and confirm the orientation of the driver without seeing the driver and/or screw.

Abstract: Modular extractor device for removing bone cement from a bone cavity (C), including an elongated body with an axis of symmetry (X-X), a proximal end, arranged during use at the opening of the bone cavity (C), and a distal end, arranged during use at the innermost part of the bone cavity (C). The elongated body is partially hollow and is adapted to be inserted in said bone cavity (C) filled with bone cement. The elongated body includes a plurality of rigid elements coaxial to the axis (X-X) of said elongated body, partially hollow and anchored together. At least two adjacent rigid elements include a first main section, a second main section and a flange. A main section of at least one rigid element is inserted and held in position in a main section of the other rigid element of the at least two rigid elements.

Abstract: The invention is based on a tool device, in particular hand-held tool device, for use in a surgical method, comprising a tool receptacle, an operating unit, a torque limitation unit, a torque transmission unit and a magazine unit. The torque limitation unit is arranged between the operating unit and the tool receptacle and comprises a plurality of torque limitation elements which are provided to be destroyed when a given torque is exceeded. The magazine unit is provided to exert a thrust force onto the torque limitation elements for introducing them one by one into the torque transmission unit, and the torque limitation unit is provided to respectively receive a torque limitation element and to destroy it when the given torque is exceeded, wherein the torque limitation elements are arranged on a rotary working axle of the tool receptacle.

Abstract: Devices and methods are provided for ablational treatment of regions of the digestive tract in post-bariatric surgery patients who fail to achieve or maintain the desired weight loss. Bariatric procedures include Roux-en-Y gastric bypass, biliopancreatic diversion, and sleeve gastrectomy. These procedures reconstruct gastrointestinal tract features, creating pouches, stoma, and tubes that restrict and/or divert the digestive flow. Post-surgical dilation of altered structures is common and diminishes their bariatric effectiveness. Ablation of compromised structures can reduce their size and compliance, restoring bariatric effectiveness. Ablation, as provided the invention, starts at the mucosa and penetrates deeper into the gastrointestinal wall in a controlled manner. Control may also be provided by a fractional ablation that ablates some tissue within a target region and leaves a portion substantially unaffected.

Abstract: A handpiece for injecting steam into a human or animal vessel in order to heat the vessel, including a steam generator for generating steam from a liquid and a connection member for connecting a catheter or a needle that is to inject the steam into the vessel. The steam generator includes a reservoir to contain the liquid, the reservoir being equipped with electrical heating means for heating the liquid in order to vaporize it and produce a stream of steam that diffuses via the connection member. The steam generator also includes a first nonreturn outlet valve interposed between the reservoir and the connection member for preventing fluid from passing from the connection member toward the reservoir. The first irst nonreturn outlet valve being a pressure-regulating valve which opens to allow steam to pass from the reservoir toward the connector when the pressure in the reservoir has reached a threshold value.

Abstract: In a plasma treatment system, a coefficient K which is a ratio of a supply amount and a suction amount of saline and also a minimal water amount required for generation of plasma is provided, and the required supply amount and suction amount of the saline are set from the coefficient K acquired on the basis of an output level of high-frequency energy, thereby performing a plasma treatment.

Abstract: An apparatus and procedure for defining the area for a thermo-electric knife to perform a bloodless intrastromal abdominal hysterectomy procedure while minimizing damage to the pericervical ring. The apparatus is configured to be inserted into the center cavity of the cervix and uterus to engage the uterine wall. The apparatus comprises an elongate member having a first end configured to extend into the center cavity of the uterus and cervix, and a thermo-electric knife guide plate secured concentrically to the elongate member proximal to the second end of the member to define the area for dissection of connective tissue between the cervix and the pericervical ring by a thermo-electric knife.

Abstract: A method of electrothermally fusing together pieces of tissue at an interface and simultaneously cutting the fused tissue along a linear path through the interface, including: compressing the tissue pieces together at the interface sufficiently for fusing the tissue pieces together and for cutting the fused tissue pieces in the linear path through the fused tissue at the interface; delivering an impulse of electrical power of no greater than 4.0 seconds time duration which contains sufficient energy to fuse the tissue pieces together at the interface and to simultaneously cut the fused tissue; converting the electrical power impulse into thermal energy applied at the interface; and regulating the temperature of the thermal energy applied at the interface in a range of 200° C. to 320° C. while fusing and simultaneously cutting the tissue pieces at the interface by controlling characteristics of the electrical power impulse.

Abstract: The present disclosure relates to devices, systems and methods for evaluating the success of a treatment applied to tissue in a patient, such as a radio frequency ablative treatment used to neuromodulate nerves associated with the renal artery. A system monitors parameters or values generated during the course of a treatment. Feedback provided to an operator is based on the monitored values and relates to an assessment of the likelihood that a completed treatment was technically successful. In other embodiments, parameters or values generated during the course of an incomplete treatment (such as due to high temperature or high impedance conditions) may be evaluated to provide additional instructions or feedback to an operator.

Abstract: A portable, battery powered electrosurgical wave generator is usable in performing electrically driven medical procedures. The wave generator can be small and lightweight to enable a user to carry and use the wave generator in non-operating room type settings. The wave generator can include a control unit that generates output signals in each of a cutting mode, coagulation mode, and a bipolar mode. The control unit can use a single circuit structure to generate the output signals for the cutting, coagulation, and bipolar modes. The output signals can be generated solely from a voltage produced by an incorporated battery within the generator.

Abstract: An electrosurgical instrument (1) is disclosed including a housing (2) comprising an elongate main body (3), extending in an axial direction and a grippable member (12). An implement (4) is fixed relative to and projecting from a forward region of the main body (3). A smoke evacuation passage (8) is defined within the main body (3) and extends from an inlet proximal to the implement (4). An electrical conductor (11) is housed within the housing (2) for supplying an electro-surgical current to the implement (4). The grippable member (12) is slidably connected to the main body (3) such that the axial position of the grippable member (12) relative to the main body (3) may be adjusted in use. Further there is provided a controllable smoke passage obstructor (25) for enabling adjustment of the throughput of the smoke passing through the interior of the housing (2).

Abstract: A rotation structure of an electrosurgical pen includes a pen body and a cutting tip mounted to the pen body, an extendible/retractable smoke suction tube, and a rotation assembly mounted to an end of the pen body, and a conduit rotatably coupled to the rotation assembly. The pen body has an end on which a rotary joint part is formed. The rotation assembly includes inner and outer annular members that are rotatable with respect to each other. The rotation assembly is fit over and rotatably coupled to the rotary joint part. The conduit is fit over an outer circumference of the outer annular member. In a use of the electrosurgical pen, the rotation assembly allows the smoke suction tube and the conduit to rotate relative to each other so as to allow for free rotation of the electrosurgical pen to facilitate the operation of the electrosurgical pen.

Abstract: A forceps includes a pair of shaft members, a pair of jaw members each including a distal body and a proximal flange, and a pair of electrode plates. The proximal flanges are engaged with the respective shaft members and pivotably coupled to each other such that pivoting the shaft members pivots the distal jaw bodies. The electrode plates each includes a tissue-contacting portion disposed on the distal body of the respective jaw member and a proximal extension portion extending at least partially through the proximal flange of the respective jaw member. The tissue-contacting portion and proximal extension portion of the first electrode plate are disposed in perpendicular planes relative to each other. Likewise, the tissue-contacting portion and proximal extension portion of the second electrode plate are disposed in perpendicular planes relative to each other.

Abstract: An electrosurgical instrument, a guiding catheter and a method for inserting an applicator into body lumina along a direction of insertion. The electrosurgical instrument includes a guiding catheter for inserting an applicator into body lumina along a direction of insertion and a counter sleeve, wherein the counter sleeve and the guiding catheter are arranged axially displaceably in relation to one another, and the guiding catheter in a distal region has at least one radial suction opening and the electrosurgical instrument is designed to produce a negative pressure in the guiding catheter, and wherein, furthermore, a cutting element is arranged on the suction opening and/or a distal end of the counter sleeve.

Abstract: An embodiment of an elongate medical device may comprise a shaft body having a distal end portion and a proximal end portion and three or more deflection wire assemblies, each deflection wire assembly comprising a flat wire coupled to the distal end portion and configured to deflect the distal end portion. Each flat wire may have a respective length defining a respective deflection radius, wherein each deflection radius is different.

Abstract: A medical device system is disclosed including a high-density arrangement of transducers, which may be configured to ablate, stimulate, or sense characteristics of tissue inside a bodily cavity, such as an intra-cardiac cavity. High-density arrangements of transducers may be achieved, at least in part, by overlapping elongate members on which the transducers are located, and varying sizes, shapes, or both of the transducers, especially in view of the overlapping of the elongate members. Also, the high-density arrangements of transducers may be achieved, at least in part, by including one or more recessed portions in an elongate member in order to expose one or more transducers on an underlying elongate member in a region adjacent an elongate-member-overlap region.

Abstract: EMR applicators of an EMR applicator array are provided in an openable applicator housing to allow easy patient entrance to and exit therefrom so that the portion of the patient's body that contains the tissue to be treated can be positioned directly into the applicator housing without the applicator housing having to be moved along the patient's body. This can eliminate or reduce the need for full body supporting structure as part of the applicator housing. The applicator housing provides support for the portion of the body positioned therein, and support pads or pillows, separate from the applicator housing, can replace the need for a full body support as part of the applicator housing. The housing can reduce the size and complication of prior art applicator housings, and can be placed along with the patient, on a patient support surface, such as in a standard MRI system.