Abstract: An intraosseous device comprises a stylet with a pointed end for penetrating bone and a cannula through which the stylet extends. The stylet has a bent portion which is engaged in a receiver in a handle cover. The cannula has an outwardly extending flare which is engaged in a corresponding seat in a hub. The handle and the hub have formations which interlock with one another when the tip of the stylet is aligned with the tip of the cannula. The interlock formations further assist torque transmission. The configuration ensures that the maximum manual torque can be applied to penetrate bone whilst ensuring that the stylet and cannula are aligned for maximum cutting efficiency and remain fixed to the handle and the hub respectively.

Abstract: A surgical access attachment for use with a surgical access device is disclosed. The surgical access attachment includes a ring and an access portion assembly. The ring is configured to engage a proximal portion of a surgical access device. The access portion assembly includes at least one flexible tab having an engagement structure. The engagement structure is configured to selectively engage the ring. The access portion assembly is configured to retain a seal. The access portion assembly is configured to disengage from the ring in response to a predetermined amount of force exerted on one flexible tab of the at least one flexible tab.

Abstract: A suture system including a suture construct having a first reduction construct configured to be selectively arranged in an expanded state and a reduced state. The first reduction construct includes a first locking limb, a first contractible loop, and a first opposed loop disposed generally opposite to the first contractible loop, wherein reduction of the first opposed loop contracts the first contractible loop from the expanded state into the reduced state and secures the suture construct in the reduced state. The suture construct may also include a second reduction construct. Optionally, the suture system includes a first and a second pusher tube defining a first and a second lumen, respectively, wherein each pusher tubes are advanced over portions of opposed loops, respectively, and wherein distal portions of opposed loops extend beyond the pusher tubes, respectively.

Abstract: Systems and methods of manufacture for bone and joint stabilization devices are described for such devices that are tensioned after anchoring during a medical procedure and remain active in maintaining axial tension for continued compression of the subject anatomy.

Abstract: A surgical instrument comprises a first arm connected with a longitudinal element and a first spinal construct. The first arm is connected with the longitudinal element and includes a body engageable with a first spinal construct and rotatable relative to the first arm in a first orientation and a second orientation. A second arm is axially translatable relative to the first arm and includes a body engageable with a second spinal construct and is rotatable relative to the second arm in a first orientation and a second orientation. The bodies include locks. In some embodiments, spinal constructs, implants, systems and methods are disclosed.

Abstract: A surgical instrument includes a first arm engageable with a first spinal construct disposed with a first vertebral surface. A second arm is connected with the first arm via a pivot and being engageable with a second spinal construct disposed with a second vertebral surface. The first arm is movable to rotate the first spinal construct relative to the pivot and/or the second arm is movable to rotate the second spinal construct relative to the pivot such that the first vertebral surface is moved relative to the second vertebral surface. Systems and methods of use are disclosed.

Abstract: A spinal construct comprises a first member engageable with a receiver of a first fastener having a shaft fixed with tissue. A second member is engageable with a receiver of a second fastener having a shaft fixed with the tissue. A longitudinal element connects the members. At least one of the members includes a mating element that is releasably engageable with a surgical instrument to manipulate the tissue such that movement of the receivers relative to the shafts is resisted and/or prevented. Surgical instruments, implants, systems and methods are disclosed.

Abstract: A vertebral anchor device comprising a bone anchor screw having a screw body and a screw head for coupling a link element to the screw body, the screw head being mounted to move on the screw body; the screw body comprising a threaded shank of a longitudinal axis AA for anchoring the screw body in a vertebra, and provided at one of its ends with a coupling head for coupling the screw body to the screw head; the screw head comprising a head body of a longitudinal axis BB and through which a channel passes longitudinally that is suitable for receiving, in the head body bottom portion, the coupling head; said vertebral anchor device further comprising assembly means for assembling together the coupling head and the screw head, the coupling head having a portion of cylindrical shape and of axis perpendicular to the threaded shank.

Abstract: A spinal implant for immobilizing the C1 vertebra with respect to the C2 vertebra of the spine provides controlled coupling between the C1 and C2 vertebrae, and includes a C1 component attachable to the C1 vertebra, two C2 components attachable to the C2 vertebra, and a transverse element. The C1 component has two wings each of which retains a rod holder that rotates and translates for capturing a C2 component rod. Each C2 component has a hook for connection with a side of the C2 vertebra lamina and a rod for attachment to one of the rod holders of the C1 component. Each C2 component receives and secures the transverse connector which holds position of the C2 components relative to one another. Each C2 component may include a plate configured for compression against the C2 vertebra spinous process, with each plate including spikes to aid in preventing construct migration.

Abstract: A spinal implant for immobilizing the C1 vertebra with respect to the C2 vertebra of the spine provides controlled coupling between the C1 and C2 vertebrae, and includes a C1 component attachable to the C1 vertebra, two C2 components attachable to the C2 vertebra, and a transverse element. The C1 component has two wings each of which retains a rod holder that rotates and translate for capturing a C2 component rod. Each C2 component has a hook for connection with a side of the C2 vertebra lamina and a rod for attachment to one of the rod holders of the C1 component. Each C2 component receives and secures the transverse connector which holds position of the C2 components relative to one another. Each C2 component may include a plate configured for compression against the C2 vertebra spinous process, with each plate including spikes to aid in preventing construct migration.

Abstract: The present invention relates to an interspinous integration type implant.

Abstract: The present invention relates to an instrument for band coupling between spinous processes that comprises: a needle unit that is inserted through a cutaway insertion portion of a patient's abdomen and is discharged through a cutaway discharge portion of the abdomen while passing between a spinous process protruding from the spine and a neighboring spinous process; and a band unit that is detachably coupled to an end portion of the needle unit and has a predetermined level of tension, the band unit being disposed between the spinous process and the neighboring spinous process, outside the spinous process, and outside the neighboring spinous process to secure the spinous process and the neighboring spinous process together. Thanks to the relatively cheap and simple configuration, it is possible to effectively conduct a procedure irrespective of proficiency, acquire an optimal procedure result, and cope with various patients' body types.

Abstract: Devices and methods for positioning and immobilizing at least two adjacent vertebrae using adjacent spinous processes. The method includes positioning a spinous process fusion device in an interspinous space between adjacent spinous processes including a rod and a first wing, and attaching a second wing to the rod, for example, using a ratcheting mechanism.

Abstract: A spacer for laminoplasty is provided, the spacer including: a first spacer fixed to an upper lamina plate in a state in which an incision surface of the upper laminate plate of a lamina plate of an incised cervical vertebrae is seated on and supported by the first spacer; and a second spacer fixed to a lower lamina plate so that an incision surface of the lower lamina plate of the lamina plate of the incised cervical vertebrae is in contact with and supported by the second spacer, wherein the first spacer and the second spacer are in a coupled state in which they are not separated from each other by a fixed bar, while having expandable lengths with respect to each other.

Abstract: A surgical instrument comprises a fulcrum including a first surface that defines a cavity configured for disposal of a first implant support such that the fulcrum is movable relative to the support. The first surface is rotatable relative to the fulcrum to engage the support and fix the first surface with the support. A second surface is engageable with a second implant support. In some embodiments, spinal constructs, implants, systems and methods are disclosed.

Abstract: Internal bone fixation devices and methods for using the devices for repairing a weakened or fractured bone are disclosed herein. A device for use in repairing a fractured bone includes a delivery catheter having an elongated shaft with a proximal end, a distal end, and a longitudinal axis therebetween, wherein the delivery catheter has an inner void for passage of at least one reinforcing material and an inner lumen for passage of a light source; a conformable member releasably engaging the distal end of the delivery catheter, wherein the conformable member moves from a deflated state to an inflated state when the at least one reinforcing material is delivered to the conformable member; and an adapter releasably engaging the proximal end of the delivery catheter for receiving the light source and the at least one reinforcing material.

Abstract: An anchoring system for the implantation of at least one anchoring device in at least one preferably bone tissue, the system is disclosed, with some embodiments comprising: at least one anchoring device comprising a curved body extending between an anterior end intended to penetrate without any deformation in the bone tissue and a posterior end intended to remain turned outward of the bone tissue, at least one guide extending along a longitudinal axis between a posterior end and an anterior end and comprising at least one guiding surface, substantially along the longitudinal axis, able to guide at least one anchoring device.

Abstract: Device (1) for applying bone replacement pastes or bone cements, wherein the device (1) comprises: A) a container-like base part (4) with a first end (5), a second end (6) and a cavity (7), which defines a first longitudinal axis (3), is closed at the first end (5) and is open at the second end (6); and B) a filling piston (8) which can be inserted slidably into the cavity (7) and has a second longitudinal axis (10) and two or more hollow spaces (9) which extend through the filling piston (8) coaxially or parallel to the second longitudinal axis (10) and into which the cannula (13) of the applicator (2) can optionally be inserted.

Abstract: Storage and mixing systems and methods for pasty multicomponent polymethylmethacrylate bone cements, the systems and methods comprise a first tubular cartridge with a first cylindrical internal space containing a first starting component, a first dispensing plunger, a second tubular cartridge that is arranged within the first tubular cartridge. The external wall of the second cartridge touches against the internal wall of the first cartridge and is attached to the internal wall of the first cartridge, whereby the second cartridge contains a second starting component and has a second dispensing plunger arranged in it, whereby a pressing device with a clamping edge for compressing the second cartridge that can be propelled axially in the internal space of the first cartridge is arranged, as seen from the cartridge head, behind the first dispensing plunger and the second dispensing plunger.

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

Abstract: An orthopedic screw extractor device including a shaft, an end portion about a first end of the shaft for securing to a handle, and a screw extracting tip about a second end of the shaft opposite the first end. The screw extracting tip further includes a generally frustoconical shape having a side at an angle of about 5 to 15 degrees relative to a longitudinal axis of the screw extracting tip. The screw extracting tip further includes first, second and third screw threads and first, second and third flutes circumferentially spaced about the screw extracting tip and extending across an entire length of the screw extracting tip. Each of the screw threads has a lead of about 0.07 to 0.12 inches, a pitch of about 0.02 to 0.04 inches, a thread angle of about 40 to 50 degrees, and a depth of about 0.01 to 0.02 inches.

Abstract: An ablation catheter comprises: an elongated catheter body extending longitudinally between a proximal end and a distal end along a longitudinal axis; a distal member disposed adjacent the distal end, the distal member including an ablation element to ablate a biological member; one or more acoustic transducers disposed in the distal member and each configured to direct an acoustic signal toward a respective target ablation region and receive reflection echoes therefrom; and an acoustic redirection member disposed in the distal member to at least partially redirect the acoustic signal from at least one of the acoustic transducers toward a tissue target. The distal member includes a most-distal portion, a proximal portion, and a deflectable portion between the most-distal portion and proximal portion to permit deflection between the most-distal portion and proximal portion of the distal member. The transducers and redirection member are mounted on opposite sides of the deflectable portion.

Abstract: A multi-functional electrosurgical plasma accessory having a handpiece and an extendable probe assembly. The extendable probe assembly has a shaft member, a tube, an electrode, a spacer and a collet. The shaft member and tube each may be formed of a plurality of structures assembled together, each may be of a single unitary design, or both together may be of a single unitary design. The shaft member has an interior channel, a distal end and a proximal end comprised of a neck portion at the distal end of the shaft member, a grip. The elongated portion of the shaft is movable within the spacer between a first position in which a portion of a distal end of the electrode extends out of the tube and a second portion in which the distal end of the electrode does not extend out of the tube.

Abstract: A surgical energy system includes a first and second surgical instruments and a generator including a universal interface. The first surgical instrument includes a first instrument connector having one or more instrument couplers disposed in a first instrument coupler configuration. The second surgical instrument includes a second instrument connector having one or more instrument couplers disposed in a second instrument coupler configuration. The first and second instrument coupler configurations are different. The generator includes a universal interface including generator couplers arranged to provide generator coupler configurations at the universal interface. Each generator coupler configuration accommodates one of the first and second instrument coupler configurations in order to electronically couple the generator to a respective one of the first and second surgical instruments.

Abstract: An electrosurgical generator includes: a power supply configured to output a DC waveform; an inverter coupled to the power supply, the inverter including a plurality of switching elements; and a controller coupled to the inverter and configured to generate a switching angle waveform including a plurality of switching pulses. The controller is further configured to at least one of select or calculate the plurality of switching pulses to activate the plurality of switching elements to generate a radio frequency waveform based on the DC waveform and to minimize harmonics of the radio frequency waveform.

Abstract: Concepts presented herein relate to an interface module that can be electrically coupled to an electrical stimulation generator, a radio frequency generator and an instrument. A selection module is coupled to the interface module and operates in a first mode to deliver electrical stimulation signals from the electrical stimulation generator to the instrument and in a second mode to deliver radio frequency signals from the radio frequency generator to the instrument.

Abstract: Ablation systems and methods of the present disclosure are directed toward delivering pulsed radiofrequency (RF) energy to target tissue. The pulsations of the RF energy, combined with cooling at a surface of the target tissue, can advantageously promote local heat transfer in the target tissue to form lesions having dimensions larger than those that can be safely formed in tissue using non-pulsed RF energy under similar conditions.

Abstract: Ablation systems and methods of the present disclosure are directed toward delivering pulsed radiofrequency (RF) energy to target tissue. The pulsations of the RF energy, combined with cooling at a surface of the target tissue, can advantageously promote local heat transfer in the target tissue to form lesions having dimensions larger than those that can be safely formed in tissue using non-pulsed RF energy under similar conditions.

Abstract: Disclosed herein are ablation systems and methods for providing feedback on lesion formation in real-time. The methods and systems assess absorptivity of tissue based on a degree of electric coupling or contact between an ablation electrode and the tissue. The absorptivity can then be used, along with other information, including, power levels and activation times, to provide real-time feedback on the lesions being created. Feedback may be provided, for example, in the form of estimated lesion volumes and other lesion characteristics. The methods and systems can provide estimated treatment times to achieve a desired lesion characteristic for a given degree of contact, as well as depth of a lesion being created. The degree of contact may be measured using different techniques, including the phase angle techniques and a coupling index.

Abstract: A blood vessel dissecting device is disclosed, which includes at least two dissecting devices, which are inserted into a living body along a blood vessel to dissect tissue in a direction of alignment thereof with the blood vessel. The at least two dissecting devices include a first dissecting device and a second dissecting device. The first dissecting device and the second dissecting device are disposed juxtaposedly in the living body, and a branch vessel branched from the blood vessel is located between the first dissecting device and the second dissecting device.

Abstract: A blood vessel dissecting device is disclosed, which includes a dissecting device which, when being inserted into a living body along a blood vessel, dissects tissue in a direction of alignment thereof with the blood vessel, and a cutting device which, when being inserted into the living body along the blood vessel, cuts tissue surrounding the blood vessel in a direction of alignment thereof with the blood vessel. The cutting device includes a main body section which is inserted into the living body and holds the tissue between itself and the dissecting device, and a cutting section which cuts the tissue held between the main body section and the dissecting device.

Abstract: Ablation systems of the present disclosure facilitate the safe formation of wide and deep lesions. For example, ablation systems of the present disclosure can allow for the flow of irrigation fluid and blood through an expandable ablation electrode, resulting in efficient and effective cooling of the ablation electrode as the ablation electrode delivers energy at a treatment site of the patient. Additionally, or alternatively, ablation systems of the present disclosure can include a deformable ablation electrode and a plurality of sensors that, in cooperation, sense the deformation of the ablation electrode, to provide a robust indication of the extent and direction of contact between the ablation electrode and tissue at a treatment site.

Abstract: A temperature monitoring bipolar forceps may include a first forceps arm and a second forceps arm. The first forceps arm may include a first channel, a first conductor tip, and a first thermocouple housing. The second forceps arm may include a second channel, a second conductor tip, and a second thermocouple housing. A first thermocouple wire may include a first thermocouple and a second thermocouple wire may include a second thermocouple. The first thermocouple wire may be disposed in the first channel wherein the first thermocouple is disposed in the first thermocouple housing. The second thermocouple wire may be disposed in the second channel wherein the second thermocouple is disposed in the second thermocouple housing. The first thermocouple may be configured to measure a temperature of the first conductor tip and the second thermocouple may be configured to measure a temperature of the second conductor tip.

Abstract: An end effector for an electrosurgical instrument is disclosed which includes a first jaw, a first energy delivery surface, a first distal end, and a first proximal end. A second jaw of the end effector includes a second energy delivery surface, a second distal end, and a second proximal end. The end effector also includes an electrically conductive gap setting member which defines a distal gap distance between the first and second energy delivery surfaces. At least one pivot is fixed to one of the jaws to set a proximal gap distance between the first and second energy delivery surfaces. A method for making an end effector and a method for assembling an end effector for an electrosurgical instrument are also disclosed.

Abstract: An end effector for an electrosurgical instrument is disclosed which comprises a first jaw comprising a first energy delivery surface, a first distal end, and a first proximal end; and a second jaw comprising a second energy delivery surface, a second distal end, and a second proximal end, wherein the first energy delivery surface comprises a first curved portion that is outwardly curved, and the second energy delivery surface comprises a second curved portion that is inwardly curved. The first jaw or the second jaw is configured for pivotal movement between an open position and a closed position. In the open position, the first and second distal ends are separated apart. In the closed position, the first and second distal ends are in proximity. The end effector also comprises an electrically conductive member which protrudes from either the first or second jaw.

Abstract: An electrosurgical instrument includes an end effector having first and second jaws defining an electrically conductive gap setting member configured to maintain a gap between energy delivery surfaces of the first and second jaws. The first jaw comprises a first energy delivery surface, a first body, a first distal end, a first proximal end, and a first electrically conductive member protruding from the first body at the first distal end. The second jaw comprises a second energy delivery surface further comprising an aperture, a second body, a second distal end, a second proximal end, and a second electrically conductive member protruding from the second body at the second distal end. The second jaw further comprises an electrically insulative member extending through the aperture. At least one electrically conductive gap setting member is configured to maintain a gap between energy delivery surfaces of the first and second jaw.

Abstract: An end effector includes a first and second jaw member each comprising a first and second electrode. The first and second jaw members are movable relative to the other between an open position and a closed position. An electrically conductive member is located at the distal end of the first jaw member. The electrically conductive member is sized and configured to define a minimum distance between the first and second electrodes along the length of the first and second electrodes. An electrically insulative member is located on one of the first jaw member or the second jaw member. The electrically insulative member is sized and configured to engage tissue and has a dimension extending from one of the first jaw member or the second jaw member. The dimension is less than the minimum distance.

Abstract: An end effector has a first jaw member that includes a first electrode, and second jaw member that includes a second electrode, an electrically conductive member located at the distal end of either the first jaw member or the second jaw member, and an electrically insulative member located either on the first jaw member or the second jaw member. The electrically conductive member is configured to define a distance between the first and second electrodes along the length of the first and second electrodes, the electrically conductive member having a first stiffness. The electrically insulative member is located either on the first jaw member or the second jaw member and is sized and configured to engage tissue. The electrically conductive member has a first stiffness and the electrically insulative member has a second stiffness. The first stiffness is greater than the first stiffness.

Abstract: An end effector includes a grasping portion that includes a first jaw member having a first electrode, a second jaw member having a second electrode, a first electrically conductive member located either on the first jaw member or the second jaw member, and a gap setting portion having a second electrically conductive member located at the distal end of either the first jaw member or the second jaw member. The electrically insulative member is sized and configured to engage tissue and the second electrically conductive member sized and configured to define a minimum distance between the first and second electrodes.

Abstract: Devices, systems, and methods of the present disclosure can overcome physical constraints associated with catheter introduction to facilitate the use of a catheter with a large distal portion as part of a medical procedure benefiting from such a large distal portion, such as, for example, cardiac ablation. More specifically, devices, systems, and methods of the present disclosure can compress an expandable tip of a catheter from an expanded state to a compressed state along a tapered surface of an insertion sleeve for advancement of the expandable tip into vasculature of a patient. The tapered surface of the insertion sleeve can, for example, apply compressive forces at an angle against the advancing expandable tip. As compared to other approaches to the application of compressive force to an expandable tip, compressing the expandable tip using an angled force can reduce the likelihood of unintended deformation of the expandable tip.

Abstract: Methods for treating a human patient diagnosed with cancer with therapeutic neuromodulation and associated systems are disclosed herein. Sympathetic nerve activity can contribute to several cellular and physiological processes associated with the progression of cancer. One aspect of the present technology is directed to methods that attenuate neural traffic along target sympathetic nerves innervating tissue proximate a primary malignant tumor. Other aspects are directed to methods that at least partially inhibit sympathetic neural activity in a renal nerve of a patient diagnosed with cancer or who has a high risk of developing cancer. Targeted sympathetic nerve activity can be attenuated to improve a measurable physiological parameter corresponding to the progression of cancer in the patient. The attenuation can be achieved, for example, using an intravascularly positioned catheter carrying a therapeutic assembly, e.g.

Abstract: An irrigated balloon catheter for use in an ostium of a pulmonary vein, includes a flex circuit electrode assembly adapted for circumferential contact with the ostium when the balloon is inflated. Adapted for both diagnostic and therapeutic applications and procedures, the balloon catheter may be used with a lasso catheter or focal catheter. The flex circuit electrode assembly includes a substrate, a contact electrode on an outer surface of the substrate, the contact electrode having a “fishbone” configuration with a longitudinally elongated portion and a plurality of transversal fingers, and a wiring electrode on an inner surface of the substrate, and conductive vias extending through the substrate electrically coupling the contact electrode and the writing electrodes. Microelectrodes with exclusion zones are strategically positioned relative to the electrodes. The electrodes may also be split into electrode portions.

Abstract: Ablation systems and methods of the present disclosure include a catheter including one or more image sensors. The one or more image sensors can facilitate, for example, positioning an ablation electrode at a treatment site of an anatomic structure and, additionally or alternatively, can facilitate controlling delivery of therapeutic energy to a treatment site of an anatomic structure.

Abstract: Ablation systems and methods of the present disclosure control lesion depth and width such that, for example, wide and shallow lesions can be formed in target tissue in an anatomic structure of a patient during a medical procedure. Such wide and shallow lesions can be useful for treating, for example, thin tissue such as atrial tissue in atria of the heart of the patient.

Abstract: Ablation systems and methods of the present disclosure are directed toward delivering pulsed radiofrequency (RF) energy to target tissue. The pulsations of the RF energy, combined with cooling at a surface of the target tissue, can advantageously promote local heat transfer in the target tissue to form lesions having dimensions larger than those that can be safely formed in tissue using non-pulsed RF energy under similar conditions.

Abstract: Ablation systems of the present disclosure facilitate the safe formation of wide and deep lesions. For example, ablation systems of the present disclosure can allow for the flow of irrigation fluid and blood through an expandable ablation electrode, resulting in efficient and effective cooling of the ablation electrode as the ablation electrode delivers energy at a treatment site of the patient. Additionally, or alternatively, ablation systems of the present disclosure can include a deformable ablation electrode and a plurality of sensors that, in cooperation, sense the deformation of the ablation electrode, to provide a robust indication of the extent and direction of contact between the ablation electrode and tissue at a treatment site.

Abstract: Ablation systems of the present disclosure facilitate the safe formation of wide and deep lesions. For example, ablation systems of the present disclosure can allow for the flow of irrigation fluid and blood through an expandable ablation electrode, resulting in efficient and effective cooling of the ablation electrode as the ablation electrode delivers energy at a treatment site of the patient. Additionally, or alternatively, ablation systems of the present disclosure can include a deformable ablation electrode and a plurality of sensors that, in cooperation, sense the deformation of the ablation electrode, to provide a robust indication of the extent and direction of contact between the ablation electrode and tissue at a treatment site.

Abstract: Ablation systems of the present disclosure facilitate the safe formation of wide and deep lesions. For example, ablation systems of the present disclosure can allow for the flow of irrigation fluid and blood through an expandable ablation electrode, resulting in efficient and effective cooling of the ablation electrode as the ablation electrode delivers energy at a treatment site of the patient. Additionally, or alternatively, ablation systems of the present disclosure can include a deformable ablation electrode and a plurality of sensors that, in cooperation, sense the deformation of the ablation electrode, to provide a robust indication of the extent and direction of contact between the ablation electrode and tissue at a treatment site.

Abstract: Methods and apparatus for treating gastroesophageal reflex and other luminal conditions provide for delivering acoustic energy to a body lumen to remodel tissue surrounding the body lumen. In the case of treating GERD, a catheter carrying an ultrasonic or other vibrational transducer is introduced to the lower esophageal sphincter, and acoustic energy is delivered to the sphincter in order to tighten or bulk the sphincter such that reflex is reduced.

Abstract: According to one aspect of the present disclosure, a microwave antenna assembly is disclosed. The antenna assembly includes a feedline having an inner conductor, an outer conductor and an inner insulator disposed therebetween and a radiating portion including a dipole antenna having a proximal portion and a distal portion. The antenna assembly also comprises a sheath disposed over the feedline and the radiating portion defining a chamber around the feedline and the radiating portion. The chamber is adapted to circulate coolant fluid therethrough. The antenna assembly further includes a connection hub having cable connector coupled to the feedline, an inlet fluid port and an outlet fluid port. The connection hub includes a bypass tube configured to provide for flow of the coolant fluid from the cable connector directly to the outlet fluid port.