Abstract: An occlusion device includes a balloon and a catheter. The occlusion device is configured to allow blood to pass through the balloon, instead of around the balloon. By allowing the blood to pass through the balloon, constant traction against the vessel wall is achieved, regardless of flow rate, thereby mitigating distal migration. The balloon includes an orifice to allow blood flow through the balloon. The orifice is independent of the diameter of the vessel, therefore the effect of the diameter of the vessel changing during the procedure will not affect the flow rate of blood. The occlusion device enables finer titration of blood flow by varying the size of the orifice when compared to conventional solutions.

Abstract: A device for providing treatment is disclosed. The device provides proper skin electrical conductivity while still being minimally invasive by adhering to the patient's skin that also implements safety measures that off-the-shelf electrode options do not have. This device includes a graphite powder-based skin counter electrode that has a graphite powder suspended in an electrolyte gel that allows for electrochemical conduction between the graphite particles in the graphite powder. The gel is spread over a first side of a hydrogel layer. A device housing is mounted on the hydrogel layer over the first side. The device housing contains the electrolyte gel and graphite powder, defines an opening or lead opening as well as an empty expansion chamber for gaseous anodic byproduct. A metallic wire or rod extends from the electrolyte gel and through the housing opening and connects to a potentiostat. The second side of the hydrogel layer is adhered to the skin of the patient.

Abstract: A method and related system for treating a metallic surface in order to eradicate bacteria on the metallic surface using at least three electrodes and in which the metallic surface is one of the electrodes and in which a stimulation voltage is applied to the metallic surface and an accumulated charge is measured. The accumulated charge is compared to a threshold level wherein the stimulation voltage is maintained until the accumulated charge exceeds the threshold level. In at least one version, the metallic surface is that of a surgical implant.

Abstract: Orthopedic accessory tools such as multi-functional orthopedic sizing tools can include features for determination of a length and a diameter. Such features may include length markers positioned on a handle and at least one structure of increased dimension positioned on a shaft.

Abstract: A fluid container measurement system is disclosed. The fluid container measurement system is configured to suspend a load measurement assembly a distance above a support surface. The load measurement assembly houses a load cell and a measurement control circuit. The measurement control circuit is coupled to the load cell and configured to receive electrical signals indicative of a force imposed on the load cell. Electrical signals generated by the load cell indicative of the force exerted on the load cell can be used to measure the fluid container attached to the load cell linkage member.

Abstract: A method and related system for treating a metallic surface in order to eradicate bacteria on the metallic surface using at least three electrodes and in which the metallic surface is one of the electrodes and in which a stimulation voltage is applied to the metallic surface and an accumulated charge is measured. The accumulated charge is compared to a threshold level wherein the stimulation voltage is maintained until the accumulated charge exceeds the threshold level. In at least one version, the metallic surface is that of a surgical implant.

Abstract: A periprosthetic fracture repair solution that provides a variety of fracture fixation options should a fracture occur after total hip, knee, or especially a total shoulder arthroplasty, and provides associated methods and apparatus for application of provided fixation. The ability to pre-engineer fracture fixation contingent solutions into humeral components provides for a distinct clinical advantage in the planning and execution for periprosthetic fracture fixation. Said methods and apparatus include targeting devices which allow for intimate association of fixed angle locking screws in pre-drilled holes in an existing prosthetic or other components including additional fixation components. Such apparatus and methods further include the use of alignment devices and other components to allow for ease of repair of periprosthetic fractures utilizing the pre-engineered solutions.

Abstract: An apparatus for use with a needle electrode assembly used to disrupt biofilm from an implanted metallic object, such as a replacement orthopedic appliance, includes a body that retains the needle electrode assembly including a projecting needle portion projecting from a lower end of the body. A needle adjustment mechanism enables the length of the projecting needle portion to be adjusted, the needle adjustment mechanism including a spring element within the apparatus body and attached to the needle electrode assembly. The spring element has a substantially nonvariable spring constant such that constant pressure is applied to the needle electrode irrespective of the length of the needle electrode to be brought into contact with the skin of a subject and implanted metallic object, once released by the needle adjustment mechanism.

Abstract: An adhesive article that remains securely bonded to a substrate until a stimuli is applied. The article may be embodied as an adhesive tape, a bandage, or as other articles. The stimuli may be a change in temperature or application of a reduction that causes a structure within the article to break, creak, or otherwise disrupt to expose the adhesive to a solvent, such as via a difference in Coefficient of Thermal Expansion (CTE) or by exposing the article to a glass transition temperature.

Abstract: A calcaneal fracture fixation and reduction apparatus.

Abstract: A gastronomy tube includes an elongate tubular portion, a stop, and at least one wire loop. The elongate tubular portion is configured to extend along a length of an endoscope and to reversibly attach to the endoscope. The stop is at a proximal end of the elongate tubular portion. The at least one wire loop is at a distal end of the elongate tubular portion and is configured to extend distally from a distal end of the endoscope when the elongate tubular portion is attached to the endoscope.

Abstract: A dilator releasably connected with an endoscope to dilate a stricture as the dilator that is releasably connected to a portion of a cylindrical body of the endoscope passes through the stricture. The endoscopic dilator is moveable between an open position and a closed position configured to enable the dilator to be secured to the endoscope. When the dilator is in the closed position, an inner surface or a component on the inner surface of the dilator frictionally secures dilator to the portion of the cylindrical body of the endoscope. When in the open position, the dilator is not frictionally secured to the portion of the cylindrical body of the endoscope.

Abstract: A venous access port assembly having a housing base with a discharge stem, a cap, and an interior reservoir. The port assembly is provided with X-ray discernable indicia to identify an attribute of the assembly after its implantation and clearly appear on an X-ray of the patient in a manner informing the radiologist or technologist and the medical practitioner of that particular attribute. The indicia are cuts in a reservoir lining of radiopaque material such as metal where the cuts having narrow slot width are in the form of one or more sets of alphabetical letters such as “CT” in the lining's side wall or bottom wall.

Abstract: The present invention relates generally to cannula that interconnects an oxygen supply to a pair of hoses and two outlets or nasal tips, each tip having a polished opening for delivering oxygen into the nasal passage; the hose member from the supply received by the cannula via a connector to branch two oxygen carrying tubes, threading through a clasp encircling the hoses beneath the chin to stabilize the cannula and position them up or down; the hoses branching to opposing sides of the chin, behind each ear, meeting at a second clasp at the midpoint of the forehead above the bridge of a nose, wherein each tube courses along opposite sides of the nose downwardly into a bend element (i.e., a moldable and/or malleable turn) terminating into an outlet at the Ala's edge coming to rest inside respective nasal passage.

Abstract: A removable second stage biocompatible substrate filter including biocompatible implant material configured to trap second stage operative particulate matter, wherein the removable second stage biocompatible substrate filter is configured to combine with first stage operative particulate matter captured from irrigation fluid by a first stage filter, defining a combined product and the removable second stage biocompatible substrate filter is configured to be removable from a filter device container.

Abstract: An assembly for supporting and retracting machine cables, thereby protecting operational components attached to machine cables. A cable organization system includes at least one modular cable management module fixed to a mounting plate that allows mounting of the cable organization system to a machine or other surface. The system has clamps which secure machine cables. The clamps are supported on top of pivoting guide tubes. The cable management modules contain retraction systems which retract the machine cable clamps from an extended position. By utilizing retracting cable clamps on pivoting guide tubes, the system allows the use of operational components attached to secured machine cables, and organizes the machine cables, so that the machine cables do not extend out into the floor around the machine. The system redirects pulling force on the machine cables, so that operational components do not get pulled onto the floor if a passerby catches on a machine cable.

Abstract: A spinal jack adapted for installation between first and second vertebral processes, including first and second inter-expandable jack halves arranged between retracted and expanded positions. Each of the jack halves further includes gripping portions adapted for engaging the vertebral processes. A geared mechanism provides for expanding or retracting the jack halves in order to establish a corrected adjusted orientation between the processes.