Abstract: A trocar assembly for releasable engagement with an adapter assembly of a surgical stapling instrument includes a housing having a first end cap and a second end cap, a trocar member rotatably supported with the housing and movable between a retracted position and an advanced position, and a drive member rotatably supported within the housing. The trocar member includes a threaded body and defines a longitudinal channel. The drive member includes a drive portion received within the longitudinal channel of the trocar member. Rotation of the drive member causes longitudinal movement of the trocar member.

Abstract: Devices for the occlusion of body cavities, such as the embolization of vascular aneurysms and the like, and methods for making and using such devices. The devices may be comprised of novel expansile materials, novel infrastructure design, or both. The devices provided are very flexible and enable deployment with reduced or no damage to bodily tissues, conduits, cavities, etceteras.

Abstract: A system for treating tissue includes an applicator including a catheter and a control member extending therethrough, the control member longitudinally movable relative to the catheter and including an abutment structure proximate a distal end thereof, and a clip assembly releasably coupleable to a distal end of the applicator, the clip assembly including a pair of clip arms, a proximal end of each of the clip arms slidably received within a channel of a capsule and configured to be releasably coupled to the distal end of the control member so that the clip arms are movable relative to the capsule between a tissue receiving configuration and a tissue clipping configuration, the capsule including proximal tabs movable between a biased non-engaging and an engaging configuration, in which the proximal tabs engage an engaging portion of the lumen of the catheter, when the abutment structure is received within the capsule.

Abstract: A clip applier may be configured to apply a surgical clip to tissue. The clip applier may include a first jaw member, a second jaw member, and a stabilizing member, each configured to engage the surgical clip. The stabilizing member may be configured to move longitudinally with respect to the clip applier from a first position at least partially between the first and second jaw members to a second position at least partially between the first and second jaw members. The longitudinal movement of the stabilizing member may be constrained to longitudinal movement between the first and second positions. The stabilizing member may include first and second sidewalls on a distal portion, where the first and second sidewalls are configured to stabilize the surgical clip in a lateral direction. The clip applier may include a hinge pin received in a longitudinal channel of the stabilizing member.

Abstract: A tourniquet system embedded within the garment, the tourniquet system including a band, an optional bar, and an anti-pinch plate. The bar comprises an elongate portion of material having a first end portion, an intermediate portion, and a second end portion, at least one aperture formed in the bar so as to accept the band and allow the band to pass therethrough, at least one locking protrusion that extends from at least one of the first end portion or the second end portion. The anti-pinch plate includes one or more band receiving apertures formed so as to accept the band and allow the band to pass therethrough, wherein the anti-pinch plate includes one or more locking notches formed substantially along an edge portion of the anti-pinch plate, wherein the locking notches provide a means for securing at least a portion of the bar to the anti-pinch plate.

Abstract: A surgical sagittal saw blade cartridge that includes a guide bar formed from an inner layer and opposed outer plates. The inner layer comprising an outer tine extending distally from the proximal end of the guide bar. An outer surface of the outer tine forms a section of a side surface of the guide bar. A side weld may be formed along the side surface of the guide bar. The cartridge may include a blade coupled to the guide bar, the blade comprising a web disposed between the two outer plates. The blade may include a blade head integral with and located distal to the web, the head formed with teeth located distal to the guide bar, the teeth having a sufficient thickness to form a kerf able to receive the guide bar. A method of forming the cartridge is also contemplated, including welding the inner layer to the outer plates.

Abstract: This disclosure relates to assemblies and methods for repairing bone defects. The assemblies disclosed herein may be utilized for determining a dimension of a surgical site and removing bone prior to positioning a graft and/or implant at the surgical site.

Abstract: System and methods for channeling a path into bone include a trocar having a proximal end, distal end and a central channel disposed along a central axis of the trocar. The trocar includes a distal opening at or near the distal end of the trocar. The system includes a curved cannula sized to be received in the central channel, and having a curved distal end configured to be extended laterally outward from the distal opening in a curved path extending away from the trocar. The curved cannula has a central passageway having a diameter configured allow a probe to be delivered through the central passageway to a location beyond the curved path.

Abstract: Reciprocating rasps for the surgical preparation of the bone prior to the implantation of a glenoid or acetabular component with complex geometry are disclosed. Surgical methods for the use of such reciprocating rasps are also disclosed. Some of the methods include inserting a guide pin into the glenoid of the patient, advancing a reciprocating surgical rasp over the guide pin, reciprocating the surgical rasp so as to abrade bone tissue to form a cavity shaped to receive the glenoid component, and implanting the glenoid component in the cavity.

Abstract: Tool holder, in particular a milling cutter holder, which comprises a main body with a substantially oblong cylindrical shape defining a channel in which a transmission passes designed to transmit to the tool, in particular the milling cutter, a movement from the axis of a drive motor, and a gripping element for gripping the tool holder, characterized in that an intermediate part is provided arranged between the transmission and the axis of the drive motor, the intermediate part comprising means for enabling the rotatable connection of said intermediate part to the transmission and the axis of the motor, the intermediate part comprising means forming an abutment designed to lock in translation in the longitudinal direction of displacement of the axis of transmission by abutment in particular against the gripping element.

Abstract: A surgical rotational cutting tool, a surgical kit and a method of preparing a femur to receive a stem of a femoral prosthetic. The tool includes a longitudinal axis and a shaft extending along the longitudinal axis, which has a proximal end and a distal end. The tool also includes a head located at the distal end of the shaft. The head includes a pointed distal tip, a bone contacting outer surface having a portion which curves inwards toward the longitudinal axis as it approaches the tip, and a plurality of flutes. The edges of distal parts of neighboring pairs of the flutes meet to define a plurality of cutting edges which extend proximally from the pointed distal tip. A proximal part of each flute extends proximally across the curved portion.

Abstract: Methods and devices for performing an osteotomy on a bone are presented. In one example of the invention, a method of performing an osteotomy on a bone includes removing a portion of bone from a first side of the bone to create a gap on the first side of the bone; making a cut on a second side of the bone, opposite the first side; and rotating the bone from a first position to a second position to close the gap on the first side of the bone and open the cut on the second side of the bone to create a gap on the second side of the bone.

Abstract: A cutting jig and corresponding method of manufacture is provided. The jig comprises a unitary piece combining a bone cutting guide defining a cut plane and a set of fins projecting from a jig substrate and terminating in curvilinear bone-jig contact surfaces for abutting articular surface features. The curvilinear surfaces are characterized by custom patient-specific parameters derived from measurements obtained from selected image slices of a patient's joint region such that the curvilinear surfaces establish one and only one mechanical self-locking position for the unitary piece. One obtains a series of image slices of a patient's joint region, then selects a set of slices that show specified articular surface features in the joint region. Patient-specific parameters obtained from measurements of the slices specify curvilinear bone-jig contact surfaces and a cut plane.

Abstract: Methods for collapsing a tubular organ, such as the esophagus, involve inserting a device into the tubular organ, at least partially sealing off a section of the tubular organ, and drawing in the wall of the tubular organ by application of suction. The devices may be used to move the wall of the tubular organ away from an area undergoing treatment or therapy, such as to minimize damage to the tubular organ by application of radiofrequency energy or to limit temperature increase of the tubular organ.

Abstract: In some examples, an aspiration system a catheter and a fluid flow sensor. The fluid flow sensor includes a fluid inlet, a fluid outlet, and a flow oscillator. The fluid inlet is configured to receive fluid from the catheter. The flow oscillator configured to oscillate flow of the fluid through the fluid flow sensor to generate flow-induced vibrations. The fluid outlet is configured to discharge the fluid.

Abstract: Retrieval of material from vessel lumens can be improved by electrically enhancing attachment of the material to the thrombectomy system. The system can include a catheter having a distal portion configured to be positioned adjacent to a thrombus in a blood vessel, an electrode disposed at the distal portion of the catheter, and an interventional element configured to be delivered through a lumen of the catheter. The electrode and the interventional element are each configured to be electrically coupled to an extracorporeal power supply.

Abstract: A platform of devices for removing obstructions and other objects within a blood vessel or other interior lumen of an animal is provided. The system may be deployed in the lumen from a catheter(s) and the system may include a cage comprising a suction catheter comprising one or more suction openings located in the cage interior in order to draw the clot or other object into the cage interior.

Abstract: A surgical laser system comprises a laser source configured to generate laser energy; a laser fiber optically coupled to the laser source and configured to discharge the laser energy generated by the laser source; a rocker arm configured to control an orientation of the discharged laser energy; and a controller configured to control a movement of the rocker arm in response to feedback of the discharged laser energy or to pre-defined settings of the laser source.

Abstract: A nose clearing assembly for cleaning a user's nostrils includes a tube that is insertable into a nostril of user. A swab is coupled to the tube and the swab can be inserted into the user's nostril. The swab is comprised of a fluid absorbent material for absorbing fluid mucous from the user's nostril. A shovel is coupled to the tube and the shovel can be inserted into the user's nostril. The shovel lies on a plane that is oriented perpendicular to a longitudinal axis of the tube. In this way the shovel can engage, and subsequently remove, dried mucous from the user's nostril.

Abstract: In a treatment instrument, a shaft is rotatable around a predetermined rotation axis relative to the housing, and an end effector is bendably or curvably attached to the shaft. In the treatment instrument, an interlocking member is provided independently of the shaft, and a receiver is provided in such a manner that rotation of the receiver relative to the housing is restricted or that rotation of the receiver relative to the shaft is restricted. The interlocking member moves in conjunction with bending or curving movement of the end effector so that the receiver engages with the interlocking member, thereby preventing rotation of the shaft around the predetermined rotation axis.

Abstract: An amputation system includes a cutting element having a cutting blade traversing a V-shape. The V-shape has a vertex and an angle in a range of 90-120°. A rod, rigidly coupled to the cutting element, has its longitudinal axis aligned with the vertex so it bisects the angle of the V-shape. A barrel having a bore receives at least a portion of the rod therein wherein the rod's outboard end resides in the bore. An energetic energy source, positioned in the bore adjacent to the rod's outboard end, generates a pressure force that is incident on the rod's outboard end. The pressure force is one that peaks within 0.5 milliseconds to propel the rod from the bore at a velocity in a range of 300 to 1000 feet per second.

Abstract: A lateral disc cutter for morcellating and decorticating tissue of an intervertebral disc from between adjacent vertebrae. The device can be arranged in a retracted configuration for insertion via an access tube, and in an extended configuration for cutting of tissue in the target region. The blades may be extended to contact the concave endplate in an orientation that is substantially parallel to a mid-plane of the intervertebral disc. Blades of the device may be configured with a convex profile that substantially conforms to the concave shape of the endplate for enhanced contact length between the blade and the endplate.

Abstract: An ultrasonic surgical instrument that includes an ultrasonic transducer, a handle assembly supporting the ultrasonic transducer, a clamp arm assembly, and a mechanical lockout assembly. The handle assembly includes a housing and an ultrasonic blade acoustically coupled with the ultrasonic transducer. The clamp arm assembly includes a clamp arm. The mechanical lockout assembly is configured to switch between at least an unlocked configuration and a locked configuration. In the locked configuration, the handle assembly and the clamp arm assembly are not completely coupled together and the operator is physically prevented from activating the instrument using an operator input feature. In the unlocked configuration, the clamp arm assembly and the shaft assembly are completely coupled together and the operator is able to activate the instrument using the operator input feature.

Abstract: Devices for removing implanted objects from body vessels are provided. A device includes a sheath assembly having a cutting tip. The cutting tip includes a cutting surface that is adapted to cut tissue coupled to an implanted object as the cutting tip rotates. The sheath assembly further includes an outer shield carried outside of the cutting tip. The outer shield includes a distal opening, and the outer shield is translatable relative to the cutting tip from a first position to a second position and vice versa. In the first position the cutting surface of the cutting tip is disposed within the outer shield, and in the second position the cutting tip extends through the distal opening and the cutting surface is at least partially disposed outside of the outer shield.

Abstract: The present application is directed to various spinal stabilization systems and methods. The systems can include a plurality of spinal screws each having a screw head. The systems can also include one or more wires directly or indirectly connected to the screw heads of each of the spinal screws. The systems can also include one or more towers that is configured to be removably advanced over the wires. The spinal implant of the system can be configured to be positioned within the screw heads of the plurality of spinal screws.

Abstract: A pivotal bone anchor assembly includes a shank having an upper capture portion and a lower anchor portion for fixation to the bone of a patient, and a receiver having an open channel for receiving a rod and a lower cavity for pivotably supporting the capture portion in a non- locked configuration. The assembly also includes an insert positionable into the receiver separate from the capture portion and thereafter downwardly deployable by tooling to apply a frictional force toward the capture portion that holds the angular position of the shank relative to the receiver prior to locking the assembly with a closure, with exterior surfaces of the insert entering into a non-threaded frictional biased engagement with interior surfaces of the receiver to maintain the insert in the deployed position. The exterior surfaces of the insert are further disengageable from the interior surfaces of the receiver by tooling to re-establish pivotal movement between the shank and the receiver.

Abstract: A receiving part for receiving a rod for coupling the rod to a bone anchoring element includes a receiving part body including a first end and a second end, and having a substantially U-shaped recess at the first end forming a channel for receiving the rod, and an accommodation space for accommodating a head of the bone anchoring element, the accommodation space having an opening at the second end for introducing the head; and a pressure element arranged at least partially in the accommodation space, the pressure element including a first section having a second recess for receiving the rod, and a second section having a flexible portion to clamp the head, the first section and the second section being fixed relative to each other, wherein said pressure element is insertable from the opening.

Abstract: Devices and methods that allow a rod to be offset in a relatively small amount of space are disclosed herein. In some embodiments, first and second offset rods can be joined by a plate-type connector having a reduced thickness suitable for insertion into a small space, e.g., between adjacent bone anchors. In some embodiments, first and second offset rods can be joined by a curved connector that conforms to adjacent bone anchors and likewise has a reduced thickness.

Abstract: A method for attaching a flat and flexible band on at least one bone part is disclosed. The band includes two end portions. A rigid base body crossed by an opening, and a retaining part that can be inserted in the opening is employed. The retaining part is at least partially in the shape of a squeezable wedge comprising a central bore for passage of the end portions facing the flexible band, the bore having a transverse cross-section that can be deformed between a first cross-section for free passage of the end portions when the part has not been inserted in the opening and a second cross-section for locking the end portions by compression when the part is entirely or substantially entirely inserted in the opening.

Abstract: A surgical instrument system comprises surgical instruments for use with an implantable interspinous device having at least one pair of wings for securing the implantable device to a spinous process. The instrument system may include a surgical instrument for expanding or spreading the pair of wings to accommodate the spinous process. Further, a surgical instrument may be provided for crimping or compressing the pair of wings against the spinous process for secure attachment of the device to a vertebra. The surgical instruments may be configured similar to pliers and apply force to the pair of wings within a predetermined range so as to avoid damage, weakening or breakage of the pair of wings. The surgical instrument system may also include interspinous devices of differing sizes.

Abstract: An anchor can be coupleable to a bone, where the anchor includes a head, a shank, a first extension, and a second extension. The head can include a distal head portion and a proximal head portion, where the proximal head portion can be open at a proximal end of the head. The shank can extend distally from the distal head portion, where the shank including a threaded portion configured to engage the bone. The second extension can be opposing the first extension, and the second extension can include a second proximal support coupled to a second end of a first elongate portion, where a first proximal support can extend transverse to the longitudinal axis, and the first proximal support portion and the second proximal support portion can be separated in a first condition and can be engaged to transfer forces there between in a second.

Abstract: Apparatus and devices for adding an additional spinal construct in a patient are disclosed. In one arrangement the additional spinal construct extends an existing spinal construct ipsilaterally with an inline rod connector in a minimally invasive or preferably, percutaneous procedure. In another arrangement, the ipsilateral extension of an existing spinal construct uses an offset rod connector for receiving an additional spinal rod that may be placed interiorly or exteriorly of the existing spinal construct.

Abstract: The present invention is about an intra-corporal telescopic osteodistraction device 1 for locking the length of the bone 3 and for providing axial, torsional and bending stability; an extra-corporal force producing device 4a, 4b for producing a force for extension causing a lengthening of the intra-corporal device 1 and the bone 3; a method for bone lengthening and a bone lengthening arrangement utilizing the devices 1 and 4a, 4b of the invention.

Abstract: Disclosed are system and methods that use at least one non-threaded anchor and an implant with at least one aperture to join boney structures, where the interaction of the head of the anchor with the implant aperture causes the anchor to move transversely with respect to an initial trajectory. This movement causes compression or distraction of the boney structures which are coupled to the anchors.

Abstract: Devices, systems, and methods for bone stabilization, especially volar distal radius stabilization. The stabilization system may include a bone plate having an elongated portion, an enlarged head portion, and a transition region connecting the elongated portion to the enlarged head portion, and the plate including a plurality of through holes. A plurality of fasteners may be configured to extend through one or more of the plurality of through holes in the bone plate and into the bone. The plate may be used to stabilize a fracture in a long bone, such as a radius.

Abstract: A bone anchor includes a shank having a free end, a longitudinal axis, a channel extending axially through the shank to the free end, the channel having a first width, and at least one opening extending through a wall of the shank, and a narrowing member including an elastically deformable portion configured to extend into the channel at or near the free end. The narrowing member is adjustable from a first configuration where the deformable portion defines an opening with a width smaller than the first width to restrict a substance from exiting through the free end, to a second configuration where the deformable portion is deformed radially outwardly to define an opening with a width that is at least the first width, while at least a portion of the shank positioned at a same axial height as the deformable portion maintains a constant outer width.

Abstract: A method is provided for stabilizing a bone. A plate is positioned over a bone. The bone plate has a polyaxial screw hole with a spherically curved seat. A bone hole is formed beneath the screw hole. A screw having a head with a spherical outer surface, and a threaded shaft with an internal cannula and a plurality of fenestrations is provided. The screw is driven through the first screw hole and into the bone hole until the outer surface of the head is supported by the spherically curved screw seat. A syringe provided with a needle is inserted into the internal cannula of the shaft of the screw. The syringe includes a bone injectable material that is injected through the needle, into the internal cannula, and out of at least one fenestration into the bone. After injection, the needle is removed from the screw shaft.

Abstract: Device for bone fixation with a head portion (5), a tapering front portion (8) and a shaft (3) between said head portion (5) and said tapering front portion (8), said shaft (3) having a distal portion (3a) adjacent to said tapering front portion (8) and a proximal portion (3b) adjacent to said head portion (5); whereby said distal portion (3a) being provided with a thread and having a constant outer diameter DA and an inner core diameter DI; at least the proximal portion (3b) of said shaft (3) has a core (2) consisting of a biologically non-degradable material with degradation rate BND and having a diameter d?DI; a sleeve (9) surrounding said core and consisting of a biologically degradable material with degradation rate BD, whereby BD>BND and said sleeve (9) being fixed to said core in a non-rotatable manner.

Abstract: A device for producing a bone cement dough from a monomer liquid and a cement powder and dispensing the bone cement dough. The device includes a cartridge holding the cement powder in an internal space. A monomer receptacle screws onto the cartridge, forms a chamber, and has a plunger with a passage that is permeable to gases and the monomer liquid but is impermeable to the cement powder and that connects the internal space to the chamber. The plunger tightly closes the internal space with the exception of the passage. A gas supply opening is arranged in the wall of the monomer receptacle. A monomer liquid container holds the monomer liquid and is located in the chamber. An opening facility opens the container, and closes the gas supply opening before opening the container. Also provided is a method for producing and dispensing the bone cement dough.

Abstract: The invention relates to a delivery system, device and method for delivering biomaterials for fracture fixation (including augmented fixation), in particular, for delivery of bone cements. The mixing system ensures the biomaterial only commences setting upon extrusion from the mixer, cannula or during injection through an appropriate internal fracture fixation device, allowing for rapid closing by the surgeon. The system also permits the surgeon to cease injecting the cement for an extended period of time before continuing the injection in another area using the same cartridge, through the simple removal of one mixer and attaching another in its place. The invention also provides a method of delivery of biomaterials to a desired implantation site.

Abstract: Cryocatheter including an elongated flexible catheter member having a short rigid catheter tip for introduction into a therapy site and a heat exchange arrangement for freezing the catheter tip to a cryo-temperature from between about ?15° C. to about ?30° C. for freezing human tissue at the therapy site. Cerebral medical procedures include inter alia employing a local ice ball for sealing a bleeding rupture in an arterial wall in the case of a stroke hemorrhage, employing a local ice ball for mapping electrical disorder foci in a brain, for example, epileptic foci, and the like.

Abstract: A method and system of providing therapy to a patient's uterus. The method can include the steps of inserting a uterine ablation device into the uterus; expanding a distal anchor; inflating a proximal balloon to pull the distal anchor proximally and seat the distal anchor against the internal os of the uterus; inflating a central balloon to seal the cervix; delivering vapor from the uterine ablation device into the uterus; and condensing the vapor on tissue within the uterus. The system can include a cervical collar adapted to place a distal portion of the device within the uterus when the cervical collar contacts an external os of the cervix.

Abstract: An apparatus for gas-assisted electrosurgery having a gas-assisted electrosurgical probe comprising a tube and an electrode within said tube, wherein a distal end portion of said electrode extends from an opening at a distal end of said tube and an electrically insulating tip connected to a distal end of said electrode. The electrically insulating tip has a substantially hemispherical distal end portion having a radius r1 and a proximal portion having a circular cross-section and a central axis of a length l1, wherein l1>r1.

Abstract: A control device for use with a treatment tool that includes a heating element to apply heat to a treatment target. The control device comprises a processor configured to set a target temperature for the heating element and to control the heating element so that temperature of the heating element follows the target temperature. The processor is configured to switch the control of the heating element from a first phase to a second phase. A first followability of the temperature of the heating element in the first phase is higher than a second followability of the temperature in the second phase. The processor is configured to terminate the controlling of following the temperature of the heating element to the target temperature when a parameter is beyond a predetermined range wherein the parameter being defined as a fluctuation between the temperature of the heating element and the target temperature.

Abstract: An electrosurgical system includes a generator, a delivery device, a return device, and a return electrode monitor (REM). The delivery device is in electrical communication with the generator and has a delivery electrode configured to deliver electrosurgical energy to tissue. The return device has a first jaw member including a first return electrode and a second jaw member including a second return electrode. The first and second jaw members are configured to capture tissue between the first and second return electrodes. The REM is disposed within the generator and is in electrical communication with the first and second return electrodes. The REM is configured to determine a size of a return contact area of the first and second return electrodes with tissue to prevent delivery of electrosurgical energy from the generator to tissue when the size of the return contact are is below a threshold size.

Abstract: An end effector for a surgical tool includes a distal clevis, first and second jaws rotatably mounted to the distal clevis at a first axle, and a proximal clevis rotatably coupled to the distal clevis at a second axle. An electrical conductor extends through the proximal clevis and terminates at the distal clevis to supply electrical energy to one or both of the first and second jaws.

Abstract: A surgical system includes an electrosurgical tool configured to be releasably coupled to a surgical robotic system having a control system. The tool has a shaft having an end effector with treatment electrodes configured to apply electrosurgical power to a tissue, and aspiration and irrigation tubes having ports in the vicinity of the electrodes. The control system can control a flow rate of an irrigation fluid based on deviation of power delivered by the electrodes to the tissue from a power set point, or based on an aspiration rate that is controlled based on tissue impedance. The tool can have first and second ports and a conduit configured to selectively provide or aspirate fluids through at least one of the ports. At least one of a flow rate and an aspiration rate are controlled by the control system based on a rotational angle of the shaft relative to a ground.

Abstract: Embodiments of the present disclosure provide an electrosurgical device. The electrosurgical device includes an electrode having a first portion whose exterior is electrically uninsulated, a second portion whose exterior is electrically insulated, and a third portion. The device includes an elongated hollow body formed by a first member and a second member. The second member is capable of rotating relative to the first member. The hollow body has an internal cavity, a front end, a rear end, an external surface, and an electrical wire arranged within the body. The hollow body is configured to reversibly receive the third portion of the electrode at the front end of the body such that electrical contact is made between the electrode and the electrical wire and the second portion of the electrode is not surrounded by the hollow body. The device includes a first button, a vacuum tube and a vacuum outlet.

Abstract: An electrosurgical device is disclosed. The electrosurgical device includes a cartridge configured to be disposed within an elongate channel of an end effector. The cartridge includes an electrode having a plurality of electrode portions disposed along a longitudinal axis of the cartridge. The electrode is configured to electrically couple to a generator. Each electrode portion of the plurality of electrode portions is configured to deliver an amount of energy to a tissue placed proximate thereto. An amount of energy delivered by a first electrode portion of the plurality of electrode portions differs from an amount of energy delivered by a second electrode portion of the plurality of electrode portions.

Abstract: Surgical systems can include evacuation systems for evacuating smoke, fluid, and/or particulates from a surgical site. A surgical evacuation system can be intelligent and may include one or more sensors for detecting one or more properties of the surgical system, evacuation system, surgical procedure, surgical site, and/or patient tissue, for example.