Apparatus, systems, and methods are provided for monitoring AF episodes, delivering ATP pulses, and/or achieving electrical isolation of the left atrial appendage (LAA) of a patient's heart and/or preventing thrombus formation after electrical isolation. For example, devices are provided that may implanted from within the left atrium, e.g., to isolate the LAA, prevent thrombus formation within the LAA, facilitate endothelialization, and/or deliver pacing.

Devices, systems, and methods for the selective positioning of an intravascular neuromodulation device are disclosed herein. Such systems can include, for example, an elongated shaft and a therapeutic assembly carried by a distal portion of the elongated shaft. The therapeutic assembly is configured for delivery within a blood vessel. The therapeutic assembly can include a pre-formed shape and can be transformable between a substantially straight delivery configuration: and a treatment configuration having the pre-formed helical shape to position the therapeutic assembly in stable contact with a wall of the body vessel. The therapeutic assembly can also include a mechanical decoupler operably connected to the therapeutic assembly that is configured to absorb at least a portion of a force exerted on the therapeutic assembly by the shaft so that the therapeutic assembly maintains a generally stationary position relative to the target site.

An electrosurgical apparatus is provided having a shaft, a handle, and at least one porous electrode. The shaft is coupled to the handle and the at least one porous electrode is coupled to a distal tip of the shaft. The at least one porous electrode conducts energy provided to the distal tip and enables fluid provided to the distal tip to pass or flow through the porous structure of the at least one electrode, such that the electrosurgical energy and the fluid are simultaneously applied to patient tissue adjacent to the at least one porous electrode. The shaft is rotatable relative to the handle of the electrosurgical apparatus to change the orientation of the at least one porous electrode relative to the handle. The shaft is extendable or retractable relative to the handle to increase or decrease the distance between the at least one porous electrode and the handle

The present disclosure provides a treatment apparatus for an endoscope, comprising: a first electrode, the first electrode including an electrical treatment part and an operating wire; a sheath, a surface of the sheath being provided with a bendable flexible conductive part, the flexible conductive part being in the form of a tube, the flexible conductive part having a gap formed in the flexible conductive part to facilitate a bend of the flexible conductive part, the surface of the sheath being communicated with an external air of the flexible conductive part through the gap; wherein the operating wire is threaded within the sheath and the electrical treatment part extends out from a front end of the sheath.

Methods and apparatuses (e.g., devices, instruments and systems, including applicator handles for use with pulse generators) for automatically and/or mechanically setting impedance matching for connecting the applicator handle with different electrode tips. These methods and apparatuses may be useful for applying therapeutic energy, including but not limited to short, high field strength electric pulses, while avoiding the risk of arcing or otherwise harming the tissue.

A device for fragmenting a surgical implant includes a cap. The cap includes a first channel extending from a first end of the cap to the second end of the cap. The device includes a first electrode, a second electrode, and an endoscope coupled with the cap.

Disclosed is a method of unilateral biportal endoscopy and a surgical instrument set used in the same. More particularly, the present invention relates to a method of unilateral biportal endoscopy which separately secures a working portal for surgical instruments and an endoscopic portal for an endoscope, thereby providing a more accurate spinal surgery, and to a surgical instrument set which can be effectively applied to the method.

A surgical instrument of the present disclosure includes: a conductive cable member formed into a cable-like shape; a conductive outer shell covering a circumference of the cable member; first and second insulating portions made of materials having higher insulation properties than the cable member and the outer shell; a projecting portion projecting from a projecting insulating portion, which is one of the first and second insulating portions, toward a recessed insulating portion, which is the other, the cable member being inserted into the projecting portion; a conductive leading end portion separated from the recessed insulating portion and the outer shell, the leading end portion being bendable using tension of the cable member with an end portion connected thereto; and a power supply cable in a cable-like shape arranged inside the first and second insulating portions for supplying an electric power from outside to the leading end portion.

Electrosurgical probes for treating tissue, and surgical procedures that make use of such probes. Such a probe includes a working element having a core member, a sheath secured to the working element, and a conductor disposed in a first internal longitudinal channel of the core member and having an active electrode coupled thereto. The sheath has a passage in which the core member is disposed, and the passage has an opening at a distal end of the sheath. The conductor is reciprocable within the sheath and adapted to carry a radio frequency current to and from the active electrode, which extends from the opening at the distal end of the sheath. An irrigation channel is defined by a second internal longitudinal channel of the core member. The electrosurgical probe is marked as disposable and not for reuse in a medical procedure performed on more than one patient.

A handheld, therapeutic electrode and connector that are compatible with high voltages from a pulse generator are disclosed. The electrode includes therapeutic terminals on a tip configured to deliver high voltage pulses safely to a patient. The electrode includes sleeves, bosses, wiring channels, and other features that maximize a minimum clearance distance (across non-conductive surfaces) and air clearance between conductive connectors themselves or the connectors and a user, thus preventing dangerous arcing. Internal surfaces and seams are taken into account. The connector and its mating outlet can include similar features to maximize clearance distance. Skirts, skirt holes, and finger stops are also employed, and they can be on either the connector or outlet, or the tip or handle of the electrode.