02nd week of 2014 patent applcation highlights part 28 |
Patent application number | Title | Published |
20140012206 | Medical Device with Sliding Frontal Attachment and Retractable Needle - A medical device having a frontal attachment and a connector housing having or attachable to an associated medical apparatus, the frontal attachment slidably engaging the connector housing and having a forwardly projecting, rearwardly biased needle and a needle retraction assembly, and the connector housing having a needle retraction cavity laterally offset from the needle in a first position, the needle retraction cavity being selectively movable relative to the frontal attachment following use to reposition the needle retraction cavity into alignment with the needle to permit retraction. | 2014-01-09 |
20140012207 | Injection System with Hidden Needles - An auto-injector confines all functional components inside an enclosed housing, to keep its needle out-of-sight, at all times. Within the housing, a needle holder positions a needle at a location. A drive mechanism then simultaneously engages the needle with a fluid source and accelerates it with a predetermined momentum for insertion into a patient. After fluid delivery, the withdrawn needle is moved to storage within the housing for subsequent disposal. | 2014-01-09 |
20140012208 | DRUG DELIVERY DEVICE - A resettable drug delivery device is provided comprising a body, a cartridge holder for receiving a cartridge, and means for releasably coupling the cartridge holder to the body or the dose setting mechanism. During an initial rotational coupling movement of the cartridge holder relative to the body or the dose setting mechanism the cartridge holder is caused to move in a first axial direction relative to the body or the dose setting mechanism and during a continued rotational coupling movement of the cartridge holder relative to the body or the dose setting mechanism the cartridge holder is caused to move in a second, contrary axial direction. | 2014-01-09 |
20140012209 | Valved Tip Catheters - The present disclosure relates to multiple embodiments of catheters which include valved openings which are normally closed to maintain a lock solution within a catheter during periods of non-use. | 2014-01-09 |
20140012210 | NEEDLE GUARD - A needle guard assembly having a resilient arm extending from a base situated to slide along the shaft of a needle. In one implementation the needle guard has an elongate containment member that rides with the resilient arm and is co-operable with the resilient arm to effectuate a covering of the entire distal tip of the needle upon the needle being retracted into the needle guard. | 2014-01-09 |
20140012211 | Device for Removing a Huber Needle from a Patient - A one-piece connector for removing a housing and needle of a Huber needle assembly from a patient. The connector has a frame that can be positioned about a surface on the housing of the needle assembly and a pair of wings that pivot toward one another to provide a gripping surface. | 2014-01-09 |
20140012212 | Sprayer - A sprayer which inhibits or prevents clogging from occurring in a nozzle when a liquid is ejected from the nozzle at least one liquid flow path through which a liquid passes, a gas flow path connectable to a source of gas and along which a gas passes for ejecting the liquid, a first liquid supply connected to the at least one liquid flow path, and a gas permeable film including a plurality of through holes disposed along at least a portion of a wall defining the at least one liquid flow path, the gas permeable film being impermeable to the liquid and permeable to the gas such that the gas introduced into the gas flow path flows through the gas permeable film and into the at least one liquid flow path, thereby atomizing the liquid. | 2014-01-09 |
20140012213 | RELEASABLE MEDICAL DRAPES - A releasable medical drape, and systems and methods having the same, includes at least a liquid-impermeable, vapor-permeable layer, a pressure-sensitive adhesive layer, and a soft-gel layer having a plurality of apertures. The soft-gel layer is configured to be disposed adjacent to a tissue site. A portion of the pressure-sensitive adhesive layer extends through the plurality of apertures in the soft-gel layer to contact the tissue site. The soft-gel layer forms a good seal with the tissue site and the pressure-sensitive adhesive layer extending through the plurality of apertures forms a firm—but releasable—coupling with the tissue site. | 2014-01-09 |
20140012214 | REDUCED PRESSURE WOUND TREATMENT SYSTEM - A reduced pressure treatment appliance is provided for treating a wound on the body of a patient. In some embodiments, the appliance comprises an overlay, which is further comprised of cup members that may be detached or cut away from the overlay so that the overlay can be adjusted in size and shape. Also, in some embodiments, the overlay is further comprised of a pressure venting valve to maintain a predetermined level of reduced pressure at the site of the wound. In other embodiments, the wound treatment appliance also includes a vacuum system to supply reduced pressure to the site of the wound in the volume under the overlay. In yet other embodiments, the treatment appliance also includes wound packing means to prevent overgrowth of the wound or to encourage growth of wound tissue into an absorbable matrix comprising the wound packing means. In still other embodiments, a suction bulb may be used to provide a source of reduced pressure to an overlay that covers the wound. Finally, methods are provided for using various embodiments of the treatment appliance. | 2014-01-09 |
20140012215 | SYSTEMS, METHODS, AND DEVICES FOR TREATING A TISSUE SITE ON A MAMMAL HAVING HAIR PROXIMATE THE TISSUE SITE - Systems, methods, and devices are presented for treating a tissue site and managing hair proximate the tissue site. A composition is provided for inhibiting, removing, or weakening hair proximate the tissue site and for providing an improved fluid seal by a flexible film drape over the tissue site. In some example embodiments, a hair-modification agent is disposed at least proximate a peripheral edge of a treatment manifold between a drape and epidermis proximate a tissue site. The hair-modification agent can be configured to flow over imperfections on the epidermis and to form a fluid seal against the epidermis, and can further be configured to at least substantially weaken hair on the epidermis as the hair encounters the hair-modification agent. | 2014-01-09 |
20140012216 | DROGUE-LIKE MENSES COLLECTION DEVICE - A disposable catamenial device for the collection of menses discharge of the female human, including: a flexible resilient menstrual cup (MC), which includes: at least two resilient ribs extending inwardly from the inner surface of the MC base; an elastic rim frame connected to the top of the ribs; a reservoir bag connected to the rim in a sealed manner for collecting the menstrual fluid; and a withdrawal string connected to the cup bottom for enabling the extraction of said MC from the vagina. The MC has a drogue like structure comprising at least two flexible ribs having arcuate vertical struts (AVS) structure connected to a flat base. The ribs are connected to the elastic rim frame with at least two flexible arcuate horizontal struts (AHS). | 2014-01-09 |
20140012217 | BREATHABLE AND LIQUID IMPERMEABLE WEB AND METHOD OF MAKING THE WEB - A method is disclosed for modifying the physical characteristics of a web which involves passing the web between at least one pair of interengaged rolls to incrementally stretch the web, and then withdrawing the incrementally stretched web from between the rolls under tension. A web modified according to the disclosed method has desirable breathability and liquid impermeability, as well as extensibility and a soft, cloth-like textured surface. | 2014-01-09 |
20140012218 | AQUEOUS-LIQUID-ABSORBABLE RESIN, AQUEOUS-LIQUID-ABSORBABLE COMPOSITION, AND ABSORBER MATERIAL AND ABSORBABLE OBJECT EACH PRODUCED USING SAME - An absorbable resin, for which a large amount of a plant-derived raw material can be used, and which has an excellent capability of absorbing an aqueous liquid, and has a good gel modulus and therefore can exhibit an excellent absorbing capability under pressurized conditions; and an absorbable composition. An absorbable resin produced by binding an oxidized polysaccharide (A1) having a carboxyl group which may be neutralized with a neutralizing agent and/or a crosslinked product thereof (A2) to a poly(meth)acrylic acid (B1) in which at least one carboxyl group may be neutralized with a neutralizing agent and/or a crosslinked product thereof (B2); or an absorbable composition produced by mixing the component (A1) and/or the component (A2) with the component (B1) and/or the component (B2). The component (A1) has a weight average molecular weight of 2,000-10,000,000. The component (A1) has an acid value of 65-850 mgKOH/g. When the component (A1) has a carboxyl group which is neutralized with a neutralizing agent, the acid value of the component (A1) before the neutralization is 65-850 mgKOH/g. | 2014-01-09 |
20140012219 | INDIVIDUALLY PACKAGED PRODUCT - An individual packing product that makes it difficult to see an absorbent product disposed therein, not staining other individual packing products, and easy to put in a bag or pocket and carry. In the individual packing product, the absorbent product having an adhesive portion in a non-skin contact region is packed with a packing sheet. The absorbent product is fixed to the inner side of the packing sheet with the adhesive portion being disposed therebetween, the packing sheet is folded with the absorbent product being disposed therein, the packing sheet has a separable colored portion on the inner side thereof, and although the colored portion can be seen from the outside of the individual packing product, the absorbent product cannot be seen from the outside of the individual packing product | 2014-01-09 |
20140012220 | Protective Underwear With Absorbent Insert - The present invention provides protective underwear including shorts and removable absorbent inserts that can be pulled away from and attached to the shorts while the shorts are pulled down but not completely removed. This allows a soiled insert to be removed, and a clean replacement insert to be installed, without having to remove the person's pants and shoes. The assembled protective underwear also looks like normal underwear from the outside and is sufficiently less bulky than a traditional adult diaper allowing it to be effectively concealed when worn under most clothing. This improvement in discreetness and convenience can make a major difference to the user, such as child or adult hoping to reduce potential embarrassment while maintain maximum levels of activity. | 2014-01-09 |
20140012221 | TAMPONS - The present invention provides a tampon adapted for use by women who experience high viscosity periods/clotted menstrual blood flow. The tampon has a body comprising an elongate mass of compressed absorbent material with a proximal end (end that is inserted first) and a distal end and wherein the proximal end/tip of the tampon is formed substantially enlarged having a greater lateral spread than the distal end of the tampon prior to wetting, and has at least one of a crater, concavity, void, open hollow, cleft or lateral crevices at the proximal end to capture and hold viscous/gelatinous menstrual fluid. | 2014-01-09 |
20140012222 | LONG TERM DRUG DELIVERY DEVICES WITH POLYURETHANE-BASED POLYMERS AND THEIR MANUFACTURE - This invention is related to the use of polyurethane-based polymer as a drug delivery device to deliver biologically active compounds at a constant rate for an extended period of time and methods of manufactures thereof. The device is very biocompatible and biostable, and is useful as an implant in patients (humans and animals) for the delivery of appropriate bioactive substances to tissues or organs. | 2014-01-09 |
20140012223 | DEVICES USING MEMBRANE MEDIATED FORWARD OSMOSIS - A drug reconstitution device, method of manufacturing the drug reconstitution device and method of producing a reconstituted drug solution using the drug reconstitution device utilizes a forward osmosis membrane element positioned within a housing of the device between an input chamber and an output chamber to draw liquid from the input chamber to the output chamber via an osmotic process. The output chamber contains draw solutes and a drug to be reconstituted to produce the reconstituted drug solution in the output chamber. | 2014-01-09 |
20140012224 | Targeted hollow gold nanostructures and methods of use - Provided are novel nanostructures comprising hollow nanospheres (HGNs) and nanotubes for use as chemical sensors, molecular specific photothermal coupling agents, and photothermal ablation compounds. The nanostructures can be used in electromagnetic radiation-induced phototherapy for treatment of cancer and other disorders. The nanostructures can also be used as a sensor that detects molecules. The nanostructures are of particular use in the fields of clinical diagnosis, clinical therapy, clinical treatment, and clinical evaluation of various diseases and disorders, manufacture of compositions for use in the treatment of various diseases and disorders, for use in molecular biology, structural biology, cell biology, molecular switches, molecular circuits, and molecular computational devices, and the manufacture thereof. The hollow gold nanospheres have a unique combination of spherical shape, small size, and strong, tunable, and narrow surface plasmon resonance absorption covering the entire visible to near IR region. | 2014-01-09 |
20140012225 | DELIVERY SYSTEM - Provided herein is a delivery system, including: (a) an optical sensor configured to detect data to create a map of a patient bodily surface; and (b) a dispenser operatively associated with the optical sensor and configured to deliver compositions (optionally including cells) to the patient bodily surface based upon the data or map. Methods of forming a tissue on a patient bodily surface of a patient in need thereof are also provided, as are methods, systems and computer program products useful for processing patient bodily surface data. | 2014-01-09 |
20140012226 | DRUG INFUSION WITH PRESSURE SENSING AND NON-CONTINUOUS FLOW FOR IDENTIFICATION OF AND INJECTION INTO FLUID-FILLED ANATOMIC SPACES - An automatic injection apparatus uses non-continuous fluid-flow of drugs to identify an intended injection site and includes a drive mechanism, a sensor and a controller for establishing fluid flow and pressure and preventing fluid flow until the pressure drops below a predetermined threshold. The pressure threshold is determined based on an internal pressure generated during an injection and more fluid will not flow until it drops below a predetermined pressure. An injection is performed to establish an initial pressure threshhold and then to stop the fluid flow into a patient until the pressure drops below a predetermined pressure which allows fluid flow to resume, thus identifying a fluid filled tissue space. The initial pressure threshold is used as a control parameter to a microprocessor below which controls the rate of injection. Fluid flows below certain pressures are also used to identify a specific location within the body during injections. | 2014-01-09 |
20140012227 | SYRINGE - The present invention relates to a syringe, particularly to a small volume syringe such as a syringe suitable for ophthalmic injections. | 2014-01-09 |
20140012228 | METHODS, DEVICES AND SYSTEMS FOR ACCESSING A HOLLOW ORGAN - The methods, devices and systems described herein relate to accessing a hollow organ with increased accuracy and safety. In one example, they relate to transseptal crossings of the atrial septal wall, preferably from the right atrium into the left atrium. Numerous different devices are described for performing access methods, each of which can be used with a piercing stylet that transitions to an atraumatic configuration after piercing the intervening tissue. | 2014-01-09 |
20140012229 | DRIVE CONTROL MECHANISMS AND AUTOMATIC INJECTORS FOR INJECTABLE CARTRIDGES - An automatic injector includes a housing having a guide, a drive control mechanism, a transmission assembly, a motor, and an energy source. The housing may further include a cartridge cover. A drive control mechanism includes a drive screw, a cartridge carrier, a plunger carrier, and one or more control transfer instruments, such as a puck or cylinder. The drive screw interfaces and connects with the plunger carrier. The automatic injector is configured to accept a variety of syringes as cartridges for drug delivery. The cartridges may be ejected from the injector and safely disposed after use, making the injector a reusable automatic injector. The reusable automatic injector may further include one or more sensors, such as a cartridge sensor and a patient sensor. The novel incorporation of the drive control mechanisms into the automatic injectors of the present invention enables a single motor and transmission assembly to drive the function of multiple components, which may include the steps of: preparation and alignment of a cartridge for injection, removal of a safety cap or needle shield, needle injection, drug dose delivery, and syringe and/or needle retraction. Methods of manufacture and methods of use are also disclosed. | 2014-01-09 |
20140012230 | METHOD AND APPARATUS FOR TREATMENT OF CARDIAC DISORDERS - The present invention is directed to systems and methods for delivering therapy for a cardiac disorder, wherein the system comprises a source for supplying a protein formulation containing a protein that is otherwise deficient in cardiac cells in a patient with a cardiac disorder, and a catheter having a proximal end and a distal end for delivering the protein formulation to the pericardial sac region of a human heart. | 2014-01-09 |
20140012231 | METHOD FOR ACCESSING A RENAL ARTERY - An elongated hollow tube guiding catheter forming a portion of a guiding catheter includes a proximal end, distal end, and distal section. The distal section includes a curved section and a straight section. The curved and straight sections are shaped for facilitating introduction and retention of the catheter into the ostium of a renal artery. The system includes a dilator inserted into the catheter hollow tube with a curved distal section of the dilator opposingly extending opposite the curved distal section of the guiding catheter hollow tube. The guiding catheter includes a side arm positioned near the guiding catheter's proximal end with a multi-way stop cock fixedly attached onto a proximal end of the side arm tube. | 2014-01-09 |
20140012232 | PRODUCTION METHOD OF MEDICAL WIRE AND MEDICAL WIRE - A production method of a medical wire includes a melting portion forming process that forms an massive melting portion in a wire end by melting and solidifying the wire end of a wire; and a joining process that contacts the melting portion with a joined part, and melts and solidifies the melting portion and the joined part to form a fusion portion, thereby joining the wire end and a joined part via a fusion portion. | 2014-01-09 |
20140012233 | WOUND THERAPY SYSTEM AND RELATED METHODS THEREFOR - A portable system for subatmospheric pressure therapy in connection with healing a surgical wound, including a wound dressing dimensioned for positioning relative to a wound bed of a subject and a subatmospheric pressure mechanism dimensioned to be carried or worn by the subject. The subatmospheric pressure mechanism includes a housing having a control unit adapted to draw a vacuum and a canister associated with the housing. The canister has a collection bag disposed therein, which is in fluid communication with the wound dressing to receive exudates from the wound bed. The collection bag is adapted to expand upon receipt of the fluids and has means to release gas from within the collection bag in connection with operation of the control unit. With this arrangement, the canister is attitude independent, i.e., the canister may be positioned on edge, on its side or on its end etc. while still maintaining operation of the control unit. The collection bag may include a hydrophobic vent or material for releasing the gases. In another embodiment, the collection bag comprises a gas permeable material. The collection bag may include one of pleats or bellows. | 2014-01-09 |
20140012234 | Stretch Valve Balloon Catheter and Methods for Producing and Using Same - A safety catheter for draining a given fluid includes a hollow stretch valve and a flexible, multi-lumen, balloon drainage catheter having a proximal catheter end, a balloon defining a balloon interior to be inflated with an inflation fluid, a drain lumen. and a balloon drainage port fluidically connecting the balloon interior to the drain lumen. The hollow stretch valve is shaped to permit the given fluid to pass therethrough and is positioned in the drain lumen to at least partially slide therein such that, in a steady state, the stretch valve prevents the inflation fluid from passing through the drainage port, and, in a stretched state when the proximal catheter end is stretched, the distal sliding portion slides within the drain lumen to permit the inflation fluid to pass through the drainage port and into the drain lumen. | 2014-01-09 |
20140012235 | Stretch Valve Balloon Catheter and Methods for Producing and Using Same - A safety balloon catheter includes a stretch valve and a balloon catheter having a proximal catheter end, a balloon defining an interior to be inflated with an inflation fluid, an inflation lumen extending through the shaft to the interior and shaped to convey inflation fluid thereto and from, a second lumen parallel to the inflation lumen, and a balloon drainage port fluidically connecting the balloon interior to the second lumen. The hollow stretch valve is shaped to permit a fluid to pass therethrough and is positioned in the second lumen to at least partially slide therein such that, in a steady state, the stretch valve prevents the inflation fluid from passing through the drainage port and, in an over-inflated state, the distal sliding portion slides within the second lumen to permit the inflation fluid to pass through the drainage port and into the second lumen. | 2014-01-09 |
20140012236 | SURGICAL ADAPTER ASSEMBLIES FOR USE BETWEEN SURGICAL HANDLE ASSEMBLY AND SURGICAL END EFFECTORS - Adapter assemblies are provided for selectively interconnecting a surgical end effector that is configured to perform at least a pair of functions and a surgical device that is configured to actuate the end effector, wherein the adapter assembly includes an adapter knob housing configured and adapted for connection with the surgical device and to be in operative communication with each of the at least one rotatable drive shaft of the surgical device, the adapter knob housing defining a lumen extending longitudinally therethrough and a ring gear formed in an inner surface of the lumen of the adapter knob housing, the ring gear defining an internal array of gear teeth which are engaged with a spur gear of a rotatable drive shaft. The adapter knob housing may be a unitary member and may be formed of plastic. | 2014-01-09 |
20140012237 | SURGICAL ADAPTER ASSEMBLIES FOR USE BETWEEN SURGICAL HANDLE ASSEMBLY AND SURGICAL END EFFECTORS - An adapter assembly is provided for selectively interconnecting a surgical end effector that is configured to perform a function and a surgical device that is configured to actuate the end effector, the end effector including at least one axially translatable drive member, and the surgical device including at least one rotatable drive shaft. The adapter assembly includes at least one drive converter assembly including a drive shaft; a drive coupling nut threadably connected to a distal end portion of the drive shaft; and an axially translatable drive bar connected to the drive coupling nut, wherein rotation of the drive shaft results in axial translation of the drive bar. The drive coupling nut engages 29 teeth of the threaded distal end portion of the drive shaft. The drive coupling nut is manufactured from unreinforced PEEK thermoplastic polymer. | 2014-01-09 |
20140012238 | SWITCH BLOCK CONTROL ASSEMBLY OF A MEDICAL DEVICE - The present disclosure provides a surgical device, comprising: a jaw assembly defining a first longitudinal axis and including a first jaw and a second jaw moveable relative to the first jaw; an elongated body defining a second longitudinal axis and coupled to a proximal end of the jaw assembly, wherein the jaw assembly is configured to articulate about an articulation axis transverse to the second longitudinal axis relative to the elongated body; a handle assembly coupled to a proximal end of the elongated body and comprising at least one motor mechanically coupled to the jaw assembly; and a control assembly coupled to the handle assembly, the control assembly including a first control button, a second control button, a first rocker device disposed about the first control button and configured to rotate thereabout, and a second rocker device disposed about the second control button and configured to rotate thereabout. | 2014-01-09 |
20140012239 | TISSUE ACCESS GUIDEWIRE SYSTEM AND METHOD - A method and system for guiding at least a portion of a surgical device to a desired position between two tissues in a patient's body involves coupling a guidewire to the device and pulling the distal end of the guidewire to guide at least a portion of the surgical device to a desired position between the two tissues. The surgical device generally includes one or more guidewire coupling members and may comprise a tissue access device. A system may include a guidewire and a surgical device. In some embodiments, a guidewire, a tissue access device, and one or more additional devices to use with the access device may be provided. Methods, devices and systems may be used in open, less-invasive or percutaneous surgical procedures, in various embodiments. | 2014-01-09 |
20140012240 | RESTORATION OF ACCOMMODATION BY LENS REFILLING - A method for refilling a lens of an eye or increasing the elasticity of a lens of an eye includes removing a central portion of the lens core through the eye's cornea, a capsulorhexis in the eye's lens capsule and a gullet extending at least partially through the cortex of the lens. The lens is then refilled with a synthetic lens material. Sufficient lens core is left in place so that the synthetic material is not in contact with a lens capsule of the eye. The synthetic material used for refilling may be selected and may be formed in a shape and thickness so as to affect the refractive characteristics of the lens. An endocapsular lenticule may be inserted in the lens to affect the refractive characteristics of the lens. | 2014-01-09 |
20140012241 | HYPERTHERMIA TREATMENT AND PROBE THEREFOR - In vivo hyperthermia treatment of a target tissue can include imaging the target tissue with a magnetic resonance imaging (MRI) system, positioning a hyperthermia treatment probe in or proximate to the target tissue based on the imaging, and heating the target tissue by the probe. During the heating, changes in temperature of a volume of tissue that includes the target tissue can be monitored with the MRI system to determine an amount of the heating applied to the target tissue, and the heating can be terminated when the amount of the heating reaches a predetermined amount. | 2014-01-09 |
20140012242 | CATHETER DEVICE INCLUDING FLOW SENSING - Devices and methods are provided for performing an ablation procedure on tissue with flow monitoring using flow sensors. The devices include a catheter, and at least one flow sensor disposed on the catheter, and a component for applying the ablation procedure. An assessment module provides an indication of the efficacy of the ablation procedure based on the flow measurement from the flow sensor. | 2014-01-09 |
20140012243 | CYROGENIC TREATMENT METHODS - Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session. | 2014-01-09 |
20140012244 | TIME-LIMITED METHODS FOR CYROGENIC TREATMENT SYSTEMS - Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session. | 2014-01-09 |
20140012245 | METHODS AND APPARATUS FOR COAGULATING AND/OR CONSTRICTING HOLLOW ANATOMICAL STRUCTURES - An energy delivering probe is used for thermally coagulating and/or constricting hollow anatomical structures (HAS) including, but not limited to, blood vessels such as perforator veins. The probe includes a shaft and an energy source. | 2014-01-09 |
20140012246 | METHOD FOR TREATING TISSUE WITH A FERROMAGNETIC THERMAL SURGICAL TOOL - An electrical conductor, such as a wire or catheter, which is coated circumferentially with a ferromagnetic material in a selected region, is fed from a high frequency alternating current source. The ferromagnetic material has a quick response in heating and cooling to the controllable power delivery. The ferromagnetic material can be used for separating tissue, coagulation, tissue destruction or achieving other desired tissue effects in numerous surgical procedures. | 2014-01-09 |
20140012247 | ENDOSCOPIC CAP ELECTRODE AND METHOD FOR USING THE SAME - An apparatus for treating tissue in a tissue treatment region. The apparatus can comprise an electrode ring having an interior perimeter and an electrode probe having a proximal end and a distal end. The distal end of the electrode probe can be structured to axially translate relative to the interior perimeter of the electrode ring. The electrode ring and the electrode probe can be operably structured to conduct current therebetween when at least one of the electrode ring and the electrode probe is energized by an energy source. Further, the energy source can be a Radio Frequency (RF) energy source, a pulsed energy source, an irreversible electroporation energy source, or a pulsed irreversible electroporation energy source. A current from the energy source can be selected to non-thermally ablate tissue in the tissue treatment region. | 2014-01-09 |
20140012248 | APPARATUS AND METHOD FOR GASTRIC BYPASS SURGERY - A medical treatment device includes an elongate member having an internal volume, a proximal end, and a distal end, the internal volume extending from the proximal end to the distal end. The medical treatment device further includes a first coupler and a second coupler, the first coupler and the second coupler coupled to the internal volume of the elongate member; a first joining member and a second joining member, the first joining member coupled to the first coupler and the second joining member coupled to the second coupler. The first joining member is configured to attach to a first biological matter location, and the second joining member is configured to attach to a second biological matter location, the second location being distal to the first location. The second coupler is configured for manipulation to align relative the first coupler such that the second biological matter location relocates adjacent the first biological matter location. The first joining member and the second joining member are configured to join the first biological matter location to the second biological matter location. | 2014-01-09 |
20140012249 | ENDOMETRIAL ABLATION DEVICES AND SYSTEMS - Systems and methods for endometrial ablation. The systems include a handle and elongated introducer sleeve extending to an expandable working end having a fluid-tight interior chamber. A thin dielectric wall surrounds at least a portion of the interior chamber and has an external surface for contacting endometrial tissue. The thin dielectric wall surrounds a collapsible-expandable frame and receives an electrically non-conductive gas. First and second polarity electrodes are exposed to the interior and exterior of the chamber, respectively. A radiofrequency power source operatively connects to the electrode arrangement to apply a radiofrequency voltage across the first and second electrodes, wherein the voltage is sufficient to initiate ionization of the neutral gas into a conductive plasma within the interior chamber, and to capacitively couple the current in the plasma across the thin dielectric wall to ablate endometrial tissue engaged by the external surface of the dielectric structure. | 2014-01-09 |
20140012250 | MICROWAVE ANTENNA - 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. | 2014-01-09 |
20140012251 | ABLATION DEVICES AND METHODS - An ablation device for denervation including a catheter delivery mechanism including an elongated tube with a distal end and a proximal end, the distal end being emplaceable within a body lumen at a target nerve region. A guide wire, at least one radiofrequency electrode, a plurality of positioning elements, and a plurality of pressing elements initially located within the tube. The electrode being deployable from the tube at the target nerve region and forming a ring-shaped structure adjacent the distal tube end. The positioning elements being deployable from the tube at the target nerve region from a position of the tube further distal than the electrode. The pressing elements being deployable from the tube more proximal than the electrode for use in pressing the deployed electrode against tissue to be ablated. | 2014-01-09 |
20140012252 | AORTIC DISSECTION SEPTAL CUTTING TOOL - The present invention relates to methods of using medical cutting tools for treating aortic septal dissections. | 2014-01-09 |
20140012253 | Variable-Output Radiofrequency Ablation Power Supply - A medical system is provided, including an ablation system having at least one ablation element and a sensor, a generator operable to deliver radiofrequency ablation energy to the ablation element. A power supply defines a duty cycle and provides a voltage to the generator, and the power supply has a duty cycle modulator and an amplitude modulator. A processor is connected to the power supply, the generator, and the sensor. The processor obtains a feedback signal from the sensor, and adjusts the duty cycle modulator and the amplitude modulator according to the feedback signal. | 2014-01-09 |
20140012254 | CARDIAC TREATMENT DEVICES AND METHODS - Devices and methods provide for ablation of cardiac tissue for treating cardiac arrhythmias such as atrial fibrillation. Although the devices and methods are often be used to ablate epicardial tissue in the vicinity of at least one pulmonary vein, various embodiments may be used to ablate other cardiac tissues in other locations on a heart. Devices generally include at least one tissue contacting member for contacting epicardial tissue and securing the ablation device to the epicardial tissue, and at least one ablation member for ablating the tissue. Various embodiments include features, such as suction apertures, which enable the device to attach to the epicardial surface with sufficient strength to allow the tissue to be stabilized via the device. For example, some embodiments may be used to stabilize a beating heart to enable a beating heart ablation procedure. Many of the devices may be introduced into a patient via minimally invasive introducer devices and the like. Although devices and methods of the invention may be used to ablate epicardial tissue to treat atrial fibrillation, they may also be used in veterinary or research contexts, to treat various heart conditions other than atrial fibrillation and/or to ablate cardiac tissue other than the epicardium. | 2014-01-09 |
20140012255 | TISSUE RESECTION DEVICE AND RELATED METHODS OF USE - A device configured to facilitate resection of tissue. The device may include a proximal end configured to be secured to a distal portion of an introduction sheath and a distal end defining an opening that may communicate with a channel extending between the proximal and distal ends. The opening may be defined by at least one straight edge. | 2014-01-09 |
20140012256 | Systems and Methods for Neuromodulation for Treatment of Pain and Other Disorders Associated with Nerve Conduction - Methods and apparatus are provided for selective destruction or temporary disruption of nerves and/or conduction pathways in a mammalian body for the treatment of pain and other disorders. Apparatus comprises catheters having electrodes for targeting and affecting nerve tissue at a cellular level to reversible and irreversible nerve poration and incapacitation. | 2014-01-09 |
20140012257 | SYSTEM AND METHOD FOR RESECTING A VALVE - A system and method for resecting a valve in a patient, in which the system includes: a proximal frame and a distal frame opposite the proximal frame, each frame including a plurality of interconnectable frame segments, in which the proximal and distal frames are separated by an adjustable distance and positionable on opposite sides of the valve; an electrode, adjacent to the valve on at least one of the proximal and distal frames, that electrosurgically resects valve tissue; a proximal chamber and a distal chamber coupled to the proximal and distal frames, respectively, that allow passage of fluid and captures at least a portion of resected valve tissue, in which each chamber selectively operates in one of a radially collapsed mode and a radially expanded mode; and a drive system that adjusts the distance between the proximal and distal frames. | 2014-01-09 |
20140012258 | METHODS AND APPARATUS FOR INTRAVASCULARLY-INDUCED NEUROMODULATION - Methods and apparatus are provided for intravascularly-induced neuromodulation using a pulsed electric field, e.g., to effectuate irreversible electroporation or electrofusion, necrosis and/or inducement of apoptosis, alteration of gene expression, changes in cytokine upregulation, etc., in target neural fibers. In some embodiments, the intravascular PEF system comprises a catheter having a pair of bipolar electrodes for delivering the PEF, with a first electrode positioned on a first side of an impedance-altering element and a second electrode positioned on an opposing side of the impedance-altering element. A length of the electrodes, as well as a separation distance between the first and second electrodes, may be specified such that, with the impedance-altering element deployed in a manner that locally increases impedance within a patient's vessel, e.g., with the impedance-altering element deployed into contact with the vessel wall at a treatment site within the patient's vasculature, a magnitude of applied voltage delivered across the bipolar electrodes necessary to achieve desired neuromodulation is reduced relative to an intravascular PEF system having similarly spaced electrodes but no (or an undeployed) impedance-altering element. In a preferred embodiment, the impedance-altering element comprises an inflatable balloon configured to locally increase impedance within a patient's vasculature. The methods and apparatus of the present invention may be used to modulate a neural fiber that contributes to renal function. | 2014-01-09 |
20140012259 | IMPLANTABLE DEVICE WITH LOCKING ADJUSTMENT MECHANISM AND METHOD FOR USING SAME - An intramedullary rod for use in a mammalian body comprising an elongate nail having a stem and a head and a threaded element carried by the head and accessible at the proximal end for rotation relative to the head. A locking mechanism coupled to the threaded element and configured to preclude rotation of the threaded element relative to the head when the locking mechanism is in a first position and permit rotation of the threaded element relative to the head when the locking mechanism is in a second position. | 2014-01-09 |
20140012260 | BONE FIXATION ASSEMBLY - A bone fixation assembly to promote healing of a bone fracture comprises a first bone engagement member and a second bone engagement member. The first bone engagement member comprises an elongated body with proximal and distal end portions, a projection, and an inner surface defining an opening. The second bone engagement member comprises a main body, first and second outer surfaces, an inner surface defining an aperture, and an inner surface defining an opening spaced from the aperture. One of the end portions of first bone engagement member is dimensioned to extend through the aperture of the second bone engagement member. The opening of the first bone engagement member and the opening of the second bone engagement member are aligned to receive a fastener when the elongated body extends through the aperture and contacts an outer surface of the second bone engagement member. | 2014-01-09 |
20140012261 | Ultrasound Enhanced Selective Tissue Removal Method and Apparatus - Method and devices for cutting and removing a portion of a tissue composition which includes cancellous bone which is directly or indirectly impinging on a neural structure of the spine by creating channels through the tissue structure and then removing the detached tissue. | 2014-01-09 |
20140012262 | SYSTEMS AND METHODS FOR PROVIDING A BONE MILLING DEVICE - A milling tool system for accurately preparing a portion of the tibia preparatory to making femoral resections. The milling too system provides a minimally invasive procedure to provide an aperture within an exposed surface of the tibia, the aperture then being used as a referencing surface to accurately resect the femur. Once the femur resections have been made, the remaining uncut portions of the tibia are exposed and easily accessible for the tibial resections. | 2014-01-09 |
20140012263 | DRIVING APPARATUSES FOR SURGICAL DEVICES AND SURGICAL DEVICES EQUIPPED WITH SUCH APPARATUSES - Driving apparatuses for surgical instruments are provided. Such apparatuses are capable of reuse without having to be sterilized in an autoclave. This reduces time as well as costs associated with surgical interventions in the areas of orthopaedic surgery and surgery related to trauma, for example. | 2014-01-09 |
20140012264 | TOTAL HIP ARTHROPLASTY - A total hip arthroplasty includes a femoral prosthesis and an acetabular prosthesis. The femoral prosthesis has a ball on a neck portion of a femoral component including a noncircular femoral body a portion coated with a porous bone ingrowth coating for noncemented fixation within a resected patient femur. The femoral body is tapered, to include a combination of a medial-lateral taper, an anterior-posterior taper, and a lateral-to-medial taper for secure seated fixation into the medullary canal of a resected femur. The acetabular prosthesis includes a hemispherical metal cup having a porous bone ingrowth surface for secure fixation within a prepared patient acetabular socket. A bearing insert is initially seated within the acetabular cup in a “trial” position without locking to determine cup placement and freedom of leg movement, and thereafter reseated in a “lock” position. A femoral broach and a bone punch tool are also provided. | 2014-01-09 |
20140012265 | ORTHOPEDIC SAW BLADE - A saw blade has a base configured for attachment with a driver, the saw being configured for cutting bone. The saw blade includes a body extending from the base to a free end, the body enclosing at least three sides of an open area adjacent the base. The blade further includes a cutting edge having a width and disposed on the body adjacent to the free end thereof and adjacent to the open area such that at least a portion of the cutting edge is disposed toward the base. The open area of the saw blade can be sized to receive a portion of a long bone therein. | 2014-01-09 |
20140012266 | METHODS AND DEVICES FOR INSTALLING STANDARD AND REVERSE SHOULDER IMPLANTS - Surgical procedures, tools and implants are disclosed for both conventional and reverse shoulder implant surgeries. The improved procedures, tools and implants relate to humeral head resurfacing, humeral head resection for standard implants, humeral head resection for reverse shoulder implants, glenoid resurfacing for standard shoulder implants and glenoid resurfacing for reverse shoulder implants. 3D scans and x-rays are used to develop virtual models of the patient anatomy, identify patient specific landmarks for anchoring guide wire installation blocks, templates and drill guides. 3D scans are also used to design patient specific tools and implants for the shoulder implant procedures and to pre-operatively determine the appropriate inclination and retroversion angles. | 2014-01-09 |
20140012267 | SYSTEM AND METHOD FOR JOINT RESURFACING AND REPAIR - An implant resection system for preparing an implant site to replace a defect in an articular surface of a first bone includes a first guide configured to be coupled generally to the first bone. The first guide includes a body portion defining a channel configured to receive a pin, wherein the pin is configured to penetrate and form a longitudinally disposed bore within the first bone. The implant resection system further includes a second guide configured to be coupled generally perpendicular to the first bone proximate to the defect by way of the bore. The second guide includes a drill bit configured to form an excision site through a portion of the articular surface in preparation of receipt of an implant. | 2014-01-09 |
20140012268 | Method And Apparatus For Preparing A Proximal Femur - A system for preparing a proximal femur can include a broach that includes a broach body having an anterior side, a posterior side, a lateral side and a medial side. The medial side can have a roughened cutting surface. The lateral side can have a smooth, non-cutting surface. The system can further comprise a cutting scribe assembly and a cutting guide assembly. | 2014-01-09 |
20140012269 | LOCKING DISTRACTOR WITH TWO-START DISTRACTION SCREW - Various exemplary embodiments relate to a distractor system including one or more of the following: a distraction screw comprising a double threaded distal portion and a nonthreaded locking feature near a proximal end of the distraction screw; a crossbar; a first arm coupled to the crossbar; a second arm coupled to the crossbar and having an interior bore sized to receive at least a portion of the distraction screw; and a lock having a nonthreaded aperture sized to receive at least a portion of the distraction screw therethrough, wherein the lock is configurable in a first position and a second position, when configured in the first position the lock engages the locking feature to substantially inhibit axial movement of the distraction screw within the interior bore, and when configured in the second position the lock substantially permits axial movement of the distraction screw within the interior bore. | 2014-01-09 |
20140012270 | JOINT STABILIZING INSTRUMENT AND METHOD OF USE - A joint spacer having a body and a series of extensions projecting therefrom is disclosed. A first of the series of extensions may include a curved section for housing a portion of a joint therein (e.g., the intercondylar notch of a knee), and a second and third of the extensions may be configured to abut an opposing portion of the joint. Once inserted, the joint spacer may maintain the spacing between, and the stabilization of, the joint during surgery. A fourth extension may be included with the spacer in which the extension may interact with an insertion-removal instrument. The insertion-removal instrument may include one end having an insertion geometry for use in inserting the spacer into the joint, and an opposing end having a removal geometry for removing the spacer. Related methods for inserting the joint spacer and various alternate joint distraction devices are also disclosed. | 2014-01-09 |
20140012271 | POLYMERIC BONE FOAM COMPOSITION AND METHOD - Biomaterials, in particular bone foams, a process for preparing such materials as well as an applicator for applying the biomaterials directly to the patient's application site, and the use of a composition comprising water, a surfactant and a propellant in the preparation of a bone foam for the preparation of a calcium phosphate foam wherein the foam is obtainable by the mixture of at least two phases, a first phase comprising water and optionally a propellant, a second phase comprising one or more sources for calcium and/or phosphate, and wherein the foaming is performed during the mixture of the at least two phases to provide an improved calcium phosphate foam, process for the preparation of a calcium phosphate foam, use of a composition, solid state structure, calcium phosphate cement foam and bone foam applicator. | 2014-01-09 |
20140012272 | TAPER DISENGAGEMENT TOOL - A kit including a first component having a male taper and a second component having an internal bore with a female taper. The first component and second component being engageable via the male and female tapers. The kit further including a disassembly tool having a body and an expandable portion separable from the body, such that the expandable portion has an initial outer diameter equal to the inner diameter of the internal bore of the second component. | 2014-01-09 |
20140012273 | CONDYLE AXIS LOCATOR - An apparatus and methods for locating the axis of rotation of one or more condyles are disclosed. A condyle axis locator can include a first concave member, a second concave member, and a handle extending between the first and second concave members. The first and second concave members can include first and second locating members, respectively, extending from a surface of the first and second concave members. The first and second locating members can each include at least one opening for receiving a marking instrument. A method for locating the axis of rotation of a condyle can include positioning a first longitudinal bone in flexion relative to an adjacent second longitudinal bone, placing one of the concave members of the condyle axis locator under the condyle, and inserting a marking instrument in the opening of the locating member to mark the axis of rotation of the condyle. | 2014-01-09 |
20140012274 | Extracapsular Surgical Procedure and Surgical Referencing Instrument Therefor - A method and device for finding isometric points in the joints of mammals for use in surgical repair of a joint. Isometric points are first identified in radiographic or other two dimensional images and then located in the actual joint. A method for repairing a cruciate ligament-deficient canine stifle employing the method and device for finding isometric points is described. A method and apparatus for locating the axis of rotation of a joint is also described. | 2014-01-09 |
20140012275 | POLYAXIAL BONE SCREW WITH SHANK ARTICULATION PRESSURE INSERT AND METHOD - A polyaxial bone screw assembly includes a threaded shank body having an upper portion, a receiver member or head, a retaining and articulating structure, and a pressure insert disposed between the shank upper portion and a rod. The receiver has a U-shaped cradle defining a channel for receiving a spinal fixation rod and a receiver cavity. The retaining and articulating structure attaches to the shank and rotates with the shank in the cavity during positioning. The pressure insert presses upon the shank upper portion and not the retaining and articulating structure. | 2014-01-09 |
20140012276 | LITHOTRIPSY EYE TREATMENT - A lithotripsy probe is used to break up cataracts, sinus blockages and other body masses, where the broken materials may be removed by suction. The lithotripsy probe may have a spark generator, a fluid motion generator, or other component for breaking up the body mass. | 2014-01-09 |
20140012277 | Intraocular Lens Delivery Systems and Methods of Use - Intraocular lens delivery devices and methods of use. | 2014-01-09 |
20140012278 | SURGICAL INSTRUMENT - A surgical instrument includes: a handpiece; a rod part at a distal end of the handpiece, the rod part including a surface for adhering a graft thereto; a hollow pipe part configured to cover the rod part, the pipe part including an inner diameter with a predetermined clearance between the pipe part and the rod part; and a moving unit configured to move the pipe part relative to the rod part along an axial direction of the rod part. | 2014-01-09 |
20140012279 | OCULAR IMPLANT APPLIER AND METHODS OF USE - Described herein is a delivery device and methods for delivering an ocular implant into an eye. The delivery device includes a proximal handle portion; a distal delivery portion coupled to a distal end of the handle portion and configured to releasably hold an ocular implant and includes a sheath positioned axially over a guidewire; and a metering system configured to provide visual guidance regarding depth of advancement of an implant positioned on the guidewire into an anatomic region of the eye. Also disclosed is a device and method for loading an implant onto the delivery device. | 2014-01-09 |
20140012280 | INTUBATION PROBE - An intubation assembly includes an intubation probe adapted to be positioned in a tear duct. The probe includes a flexible tube and a flexible wire has an end which passes through an opening in the tube. The wire is used to pull the probe into the tear duct. The transition between the wire and the tube is continuous, that is, not having any sharp edge which could become stuck in the tear duct wall when the probe is pulled by the wire during displacement from the tear duct. | 2014-01-09 |
20140012281 | EXPANDABLE GUIDE EXTENSION CATHETER - Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a guide extension catheter. The guide extension catheter may include a proximal member having a proximal outer diameter. A distal sheath member may be attached to the proximal member. The distal sheath member may have a distal outer diameter greater than the proximal outer diameter. The distal sheath member may have a proximal end, a distal end, and a longitudinal slit extending at least partially between the proximal end and the distal end. An expandable member may be attached to the distal sheath member and may extend along the longitudinal slit. The expandable member may be configured to shift between a first configuration and an expanded configuration. | 2014-01-09 |
20140012282 | ONE STEP TYMPANOSTOMY TUBE AND METHOD OF INSERTING SAME - A tympanostomy tube for insertion into and residence in a tympanic membrane of a mammal, is disclosed. The tympanostomy tube includes a body including a first end portion, a second end portion, a central portion dispensed between the first and second end portions. An axially extending passageway has a first open end disposed adjacent the first end portion, and a second open end disposed adjacent the second end portion, and an axis extending between the first open end and second open end. The first end portion includes a relatively enlarged diameter, generally radially extending flange. The central portion includes a reduced diameter portion sized for extending through and residing in tissue of the tympanic membrane. The second end portion includes a relatively enlarged diameter second flange disposed adjacent the second end portion. The second flange includes a perimetral edge having an incising portion sufficiently sharpened to cut as a knife through the tympanic membrane during insertion of the tympanostomy tube in the tympanic membrane. | 2014-01-09 |
20140012283 | ENDOSCOPE TREATMENT TOOL - An endoscope treatment tool includes a flexible sheath, a manipulation wire, and a basket portion constituted by a locking portion and a plurality of elastic wires. A maximum outside diameter portion of the basket portion is at a position closer to the locking portion than an intermediate position between a proximal end of the basket portion and the locking portion. The plurality of elastic wires is formed in a shape of a helix, and a winding pitch of the plurality of elastic wires becomes gradually smaller in a direction from a proximal side to the distal side of the manipulation wire. When a proximal side of the basket portion is reduced, an outside diameter of the maximum outside diameter portion is maintained at substantially a same size as the outside diameter before the proximal side of the basket portion is reduced. | 2014-01-09 |
20140012284 | VACUUM-ACTUATED PERCUTANEOUS INSERTION/IMPLANTATION TOOL FOR FLEXIBLE NEURAL PROBES AND INTERFACES - A flexible device insertion tool including an elongated stiffener with one or more suction ports, and a vacuum connector for interfacing the stiffener to a vacuum source, for attaching the flexible device such as a flexible neural probe to the stiffener during insertion by a suction force exerted through the suction ports to, and to release the flexible device by removing the suction force. | 2014-01-09 |
20140012285 | METHOD AND APPARATUS FOR REPLACING LEAD EXTENSION WITHOUT TUNNELING - Tether apparatus may be used to replace an implanted lead extension with a replacement lead extension without tunneling or the use of tunneling tools. | 2014-01-09 |
20140012286 | SURGICAL TOOL, SURGICAL ROBOT HAVING THE SAME, AND REMOTE CONTROL ROBOT SYSTEM - A remote control robot system includes a surgical robot having a surgical tool which is used to perform minimally invasive surgery. The surgical tool includes a detection member having a plurality of detection parts, a support member, and an optical fiber disposed between the detection member and support member. A magnitude of force and a distribution of the force may be measured by individually disposing a plurality of optical fiber bragg gratings (FBGs) below the plurality of detection parts, respectively. Accordingly, the surgical robot or the remote control robot system may provide a more precise control function and a hand-touch diagnosis function. | 2014-01-09 |
20140012287 | SURGICAL POSITIONING AND SUPPORT SYSTEM - A system for performing a medical procedure is provided comprising at least one tool and a tool support for supporting a distal portion of the tool. An operator manipulates a human interface device and produces control signals sent to a controller. The controller manipulates the tool support based on the received control signals. | 2014-01-09 |
20140012288 | INTRODUCTION DEVICES FOR HIGHLY ARTICULATED ROBOTIC PROBES AND METHODS OF PRODUCTION AND USE OF SUCH PROBES - In an introduction assembly for an articulated probe, a feeding mechanism has actuators for controlling the articulated probe. The introduction device is fixed in a positional relationship to the feeding mechanism. The introduction device includes a support member configured to support an articulated probe. A proximal end of the support member has an entrance configured to guide the articulated probe into contact with the support member. A distal end of the support member has an exit configured to guide the articulated probe from the support member into a region of interest. | 2014-01-09 |
20140012289 | APPARATUS FOR ENDOSCOPIC PROCEDURES - A surgical device is provided. The surgical device includes a jaw assembly defining a first longitudinal axis and including a first jaw and a second jaw moveable relative to the first jaw; an elongated body defining a second longitudinal axis and coupled to a proximal end of the jaw assembly, wherein the jaw assembly is configured to articulate about an articulation axis transverse to the second longitudinal axis relative to the elongated body; and a handle assembly coupled to a proximal end of the elongated body and including at least one motor mechanically coupled to the jaw assembly and a control assembly including a first control button and a second control button, wherein actuation of the first control button moves the second jaw in approximation relative to the first jaw and actuating the second control button moves the second jaw away from the first jaw, and actuating the first and second control buttons moves the jaw assembly to a centered position in which the first and second longitudinal axes are substantially aligned, the handle assembly further includes an illumination member configured to output a light pattern indicative of a status of the surgical instrument. | 2014-01-09 |
20140012290 | REMOTELY ACTUATED SURGICAL GRIPPER WITH SEIZE RESISTANCE - A surgical end effector includes a clevis and one or more jaws pivotally coupled to the clevis. At least one jaw includes a slot. An axle assembly includes a bearing axle that rotatably supports a bearing, which may be a plain bearing. An actuator coupling is coupled to the bearing axle. The bearing engages the slot such that pushing and pulling on the actuator coupling causes one jaw to close against the other jaw. The bearing axle and the jaws may be made from materials that are prone to galling and the bearing may be made from a material that resists galling. The slot may include a lip that supports the bearings in a spaced apart relationship. The bearing axle may be less than 1.5 millimeters in diameter and each bearing may be less than 3.0 millimeters in diameter. | 2014-01-09 |
20140012291 | MULTIPLE CLIP APPLIER APPARATUS AND METHOD - A surgical clip applier includes a train of clips disposed in a plane with a single clip removed from the train of clips and disposed in a staging position. A pair of jaws are adapted to receive the single clip from the staging position by operation of a jaw loader moveable outside the plane of the train of clips. In an associate method, a handle assembly is provided which is moveable in an open stroke and a closed stroke. A source of surgical clips are provided along with a pair of jaws which are adapted to receive one of the clips as the handle assembly is moved in an open stroke, the jaws are open to receive the clip. Following the opening of the jaws, a jaw loader is extended to a position between the jaws to move the clip into the jaws. The handle assembly is moveable in a closed stroke during which the jaws are closed to crimp the clip. Prior to this closing of the jaws, the jaw loader is retracted from the position between the jaws leaving the clip in the jaws. | 2014-01-09 |
20140012292 | METHOD AND APPARATUS FOR PASSING SUTURE THROUGH TISSUE - A suture passer comprising:
| 2014-01-09 |
20140012293 | LEFT ATRIAL APPENDAGE DEVICES AND METHODS - Devices and methods for clamping tissue and/or moving two tissue structures together by moving two plates or arm together. The pressure or force applied to the tissue may be used to bring the tissue together, to seal an opening or to cut through and remove a portion of the tissue. In one procedure disclosed, a clip applier may be used to apply one or more clips to the left atrial appendage of the heart to prevent clots from the left atrial appendage from embolizing and causing harm to the patient, such as a stroke. | 2014-01-09 |
20140012294 | Tissue Repair Assembly - The present disclosure relates to a tissue repair assembly. The assembly includes an interference device and a fixation device coupled to the interference device, wherein the fixation device includes a coupling portion and a capturing portion. Other assemblies and methods are also disclosed. | 2014-01-09 |
20140012295 | BLADE FOR PREPARING AN ENDOTHELIAL GRAFT, AND ASSOCIATED PREPARATION METHOD - The invention relates to an instrument for preparing an corneal endothelial graft, the tool being a trephine blade ( | 2014-01-09 |
20140012296 | Rounded-End Device, System, and Method for Preventing Posterior Capsular Opacification - Disclosed herein is an apparatus selectively attachable to an ultrasonic device to disrupt target cells from underlying tissue for treatment of an ocular condition, comprising a shaft, a coupling portion at an end of the shaft, and a cell disrupting end extending from a distal portion of the shaft. The shaft has a longitudinal axis and a first diameter. The coupling portion includes a connector portion and a hub configured to selectively couple to the ultrasonic device and impart ultrasonic vibration to the shaft. The cell disrupting end is solid and has a second diameter and a smooth, continuous, curved shape. | 2014-01-09 |
20140012297 | ULTRASONIC SURGICAL INSTRUMENTS - An ultrasonic surgical instrument is provided. The ultrasonic surgical instrument includes a housing having an elongated shaft extending therefrom. The shaft defines a longitudinal axis therethrough and has at least one jaw member disposed at a distal end thereof. The jaw member(s) is movable between open and clamping configurations. A probe extends through the shaft and operably couples to the housing, The probe includes a cutting blade at a distal end thereof adjacent the jaw member(s) to treat tissue of interest. The jaw member(s) and cutting blade are configured such that heat damage to tissue adjacent tissue of interest that has been treated by the cutting blade is reduced and/or eliminated. | 2014-01-09 |
20140012298 | ULTRASONIC SURGICAL INSTRUMENTS - An ultrasonic surgical instrument is provided. The ultrasonic surgical instrument includes a housing having an elongated shaft extending therefrom. The shaft defines a longitudinal axis therethrough and has a jaw member disposed at a distal end thereof. The jaw member is movable between an open configuration and a clamping configuration. The jaw member includes a tissue contacting surface having at least one laminate liner disposed thereon. A cutting blade extends from a distal end of the shaft and operably couples to the housing and adjacent the jaw member to treat tissue. | 2014-01-09 |
20140012299 | ULTRASONIC SURGICAL INSTRUMENTS - An ultrasonic surgical instrument is provided. The ultrasonic surgical instrument includes a housing having an elongated shaft extending therefrom. The shaft has a jaw member disposed at a distal end thereof. The jaw member is movable between an open configuration and a clamping configuration and includes a tissue contacting surface thereon. A cutting blade extends from a distal end of the shaft and operably couples to the housing and adjacent the jaw member to treat tissue. At least one sensor is configured to sense at least one operational parameter of the ultrasonic surgical instrument. At least one controller in operable communication with the at least one sensor is configured to terminate delivery of ultrasonic energy to the cutting blade when the at least one sensor senses the at least one operational parameter. | 2014-01-09 |
20140012300 | Ultrasonic Wave Generator and Method of Lipolysis - The invention relates to a device for generating an ultrasonic field having frequencies between 0.9 MHz and 4 MHz in an object, preferably in water or in human tissue, the device comprising a piezo element ( | 2014-01-09 |
20140012301 | SYSTEMS AND METHODS FOR ENDOLUMINAL VALVE CREATION - A device for manipulating tissue at a vessel includes an elongated member having a proximal end and a distal end, a guide member at the distal end of the elongated member, the guide member having a blunt distal tip for engagement against an interior wall of the vessel, and a tissue cutting device at the distal end of the elongated member, wherein the tissue cutting device has a sharp tip that is proximal to the blunt distal tip of the guide member. | 2014-01-09 |
20140012302 | FLUID EJECTION DEVICE AND MEDICAL DEVICE - A fluid ejection device includes: a pressure chamber; an actuator having a displacement plane that varies the volume of the pressure chamber; a delivery channel pipe communicating with the pressure chamber; a first reflection surface of pressure wave formed as part of a paraboloid of revolution that reflects a plane pressure wave by displacement of the actuator, the plane pressure wave propagating through the pressure chamber; and a second reflection surface of pressure wave formed as part of a paraboloid of revolution or an ellipsoid of revolution which is disposed so as to face the first reflection surface of pressure wave, wherein the first reflection surface of pressure wave and the second reflection surface of pressure wave have a common first focus, and a pressure wave reflected from the second reflection surface of pressure wave propagates through the delivery channel pipe and ejects fluid. | 2014-01-09 |
20140012303 | Braided Medical Device And Manufacturing Method Thereof - An medical implantable occlusion device ( | 2014-01-09 |
20140012304 | MULTILAYERED BALLOON - A multilayered inflatable medical appliance is disclosed. The appliance may comprise multiple adjacent layers disposed to increase total burst strength, puncture resistance or other properties. One or more layers may be comprised of a rotational spun fiber coating. Further, in some embodiments, additional top coatings may be included. Multilayered constructs may be configured with higher burst strengths and/or puncture resistance as compared to single layer constructs. | 2014-01-09 |
20140012305 | COLPOTOMY CUP-LIKE STRUCTURE AND INTRAUTERINE MANIPULATOR INCLUDING SAME - A cup-like structure for engaging a cervix of a patient includes a rim, and includes a base defining an aperture through which one or more tubular members of a uterine manipulator may extend into the uterus. The cup-like structure is made from one or more of a polyphthalamide (PPA) material and a polyetheretherketone (PEEK) material. A uterine manipulator including a cup-like structure is also disclosed. | 2014-01-09 |