28th week of 2012 patent applcation highlights part 50 |
Patent application number | Title | Published |
20120179185 | CONTACT ACTIVATED INCISION DEVICE - A contact activated incision device, comprises a housing defining a cavity, and a longitudinal axis extends between a proximal end and a distal end of the housing. A slider is slidable with respect to the housing along the longitudinal axis and at least partially positioned outside of the housing. A roller is mounted on the housing and rotatable about an axis perpendicular to the longitudinal axis. A blade assembly is mounted on the roller and has a blade, wherein the blade is movable from a retracted position to an extended position and to a final position, at the retracted position the blade is positioned in the cavity, at the extended position the blade extends at least partially beyond the proximal end of the housing, and at the final position the blade is positioned in the cavity. | 2012-07-12 |
20120179186 | Pneumatic Motor for Oscillatory Motion - The present invention is a pneumatically driven oscillatory motor. It features fan gear with an eccentrically mounted hub which imparts a wobbling motion on a bearing and associated collar. This wobbling motion then translated in to a vertical oscillatory motion of a collar arm extending radially from said collar. Additional structures to direct flow of expelled air are also provided. The collar arm may be removable from the collar. The motor has many applications where oscillatory motion is required, such as in tattoo needles. | 2012-07-12 |
20120179187 | STABILIZATION SYSTEM AND ASPIRATION DEVICE WITH PROTECTED CUTTING EDGE - A device performs a myringotomy and includes a main body, a hollow positioning member, a cutting edge for piercing a tympanic membrane, a protective sheath and an actuator. The main body is oriented along an axis and has a proximal end, a distal end and an outer surface. The main body includes an attachment hub for receiving components that provide suction. The hollow positioning member extends at least partially along the axis, is coupled to the main body and includes a distal end. The actuator is located on the main body and is configured to move the protective sheath from a first position that surrounds the cutting edge to a second position that exposes the cutting edge and from the second position back to the first position. | 2012-07-12 |
20120179188 | TRANSSEPTAL PUNCTURE APPARATUS - Devices and methods for performing a transeptal puncture procedure are described. In certain embodiments, the device includes a blunt outer needle, and a second inner needle disposed longitudinally through the lumen of the outer needle, wherein the inner needle is flexible, e.g., has a flexible portion and/or a bend or other non-traumatic conformation at its tip. | 2012-07-12 |
20120179189 | Methods and Systems for Modifying a Parameter of an Automated Procedure - A variety of systems and methods are described which enable quantitative information to be extracted regarding automated procedures, including those performed at a high speed that may require a user input, without having to interrupt the procedure. In addition, these systems and methods serve to provide information on one or more parameters of the automated procedure, whereby they may be modified, if required, to improve the automated procedure or the results from such a procedure. The systems and methods provided are especially useful in automated hair transplantation procedures. | 2012-07-12 |
20120179190 | OCCLUDER - An occluder for closing an opening in a circuit system can be transferred from a compact manifestation which extends along a longitudinal axis into an expanded manifestation. The occluder has a first expansion unit and a second expansion unit which bear on in each case one side of the opening in the expanded manifestation. Furthermore, the occluder has a first coupling part and a second coupling part which can be brought into engagement with one another, with the result that they fix the occluder in its expanded manifestation. The first coupling part has a region which extends between the first and second expansion units in the expanded manifestation. According to the invention, this region is configured such that it can expand along the longitudinal axis. It is preferably configured such that it can expand counter to a restoring force, that is to say resiliently or elastically. This occluder therefore permits automatic setting of the spacing between two expansion and/or closure units according to the structural conditions at the location of the opening to be closed. | 2012-07-12 |
20120179191 | INJECTABLE IMPLANTS FOR TISSUE AUGMENTATION AND RESTORATION - The method and device improves the functioning of dilated body parts and organs by supporting the parts and organs with an injectable and/or implantable biocompatible substance. | 2012-07-12 |
20120179192 | EMBOLIZATION DEVICE AND A METHOD OF USING THE SAME - Space-occupying devices for treating voids within the body are disclosed. The devices can have multiple elements connected to a flexible leader. The devices can be coated by a binding agent. The devices can also be fillable. Methods of making and using the devices are also disclosed. | 2012-07-12 |
20120179193 | INTRALUMINAL POLYMERIC DEVICES FOR THE TREATMENT OF ANEURYSMS - Novel medical devices and uses thereof for lining a blood vessel and/or treating an aneurysm are disclosed herein. The device comprises a non-metallic expandable tubular structure, implantable in a body vessel and being made, at least in part, from a polymeric system characterized by a stiffness which changes upon stimulation under physiological conditions. Novel polymeric systems are further disclosed herein, which are configured to produce a polymeric material upon stimulation under physiological conditions, such that a stiffness of said polymeric material is higher than a stiffness of said system. Uses of polymer systems in the manufacture of a device are further disclosed. | 2012-07-12 |
20120179194 | VASOOCCLUSIVE COIL WITH ENHANCED THERAPEUTIC STRAND STRUCTURE - A vasoocclusive coil is reinforced with a stretch resistant member to improve safety during retraction of the coil. The stretch resistant member is fixedly attached at one end to the vasoocclusive coil, and the other end of the stretch resistant member is detachably mounted to an elongated pusher member to allow for placement and release of the vasoocclusive coil within the patient's vasculature. The stretch resistant member may be formed from a therapeutic and/or bioactive non-metallic material to enhance the therapeutic properties of the vasoocclusive coil. | 2012-07-12 |
20120179195 | DUAL ENDOVASCULAR FILTER AND METHODS OF USE - Blood filter devices and methods of use. | 2012-07-12 |
20120179196 | DISTAL PROTECTION DEVICES AND METHODS OF PROVIDING DISTAL PROTECTION - A filter and methods of use to provide distal protection during a vascular procedure is provided. The filter includes a first spiral shaped support member joined to a second spiral support member to form a crossover and to form a first generally planar support frame and a second generally planar support frame. A tether is on one of the first end or the second end and a capture structure is attached to the first support frame or the second support frame. The capture structure extends in a non-planar fashion relative to the generally planar first or second support frame to which the capture structure is attached. After use to capture debris, the filter is recovered in a manner to close while maintaining captured debris within the filter. | 2012-07-12 |
20120179197 | MEDICAL INSTRUMENT - A medical instrument with a shank consisting of pivotable jaw parts and a handle, the two jaw parts of the tool are pivotable relative to each other independently via the handle and each of the pivotable jaw parts is actuated via a separate drive. One drive is designed as a grip part mounted pivotably on the handle and is connected to one jaw part via a first push/pull element mounted in an axially displaceable manner in the shank, and the other drive is an adjusting wheel rotatable about a longitudinal axis of the shank and is connected to the other jaw part of the tool via a second push/pull element mounted in an axially displaceable manner in the shank. The push/pull element is designed as a push/pull rod, and the push/pull element which is coupled to the adjusting wheel is designed as a push/pull tube coaxially surrounding the push/pull rod. | 2012-07-12 |
20120179198 | SUTURE WITH FILAMENTS FORMED OF POLYETHER-KETONE VARIANT - A high strength abrasion resistant surgical suture material with improved tie down characteristics and tissue compliance with braided yarns formed of ether-ketone variant. The suture features a multifilament jacket formed of braided yarns of ether-ketone variant, optionally braided with yarns of polyester, silk, nylon, ultrahigh molecular weight polyethylene or aramid fibers. The braided jacket surrounds a core formed of twisted yarns of ether-ketone variant or ultrahigh molecular weight polyethylene. The suture has exceptional strength, is ideally suited for most orthopedic procedures, and can be attached to a suture anchor or a curved needle. | 2012-07-12 |
20120179199 | ADJUSTABLE ANCHOR SYSTEMS AND METHODS - An adjustable anchor system provides for securing tissue to bone and includes an anchor with a collapsible suture loop affixed thereto and a tissue suture connected to the collapsible suture loop. After the tissue suture is loaded into the tissue and the anchor implanted into the bone the collapsible loop is collapsed to tension the tissue suture. | 2012-07-12 |
20120179200 | SUTURE ANCHOR WITH PULLEY - Methods and devices are provided for anchoring suture to bone. In one exemplary embodiment, a cannulated suture anchor is provided and it includes a suture-engaging member formed therein and configured to receive a suture therearound such that trailing ends of the suture can extend through the suture anchor. The present invention also provides exemplary sutures and drivers that can be used with the various methods and devices disclosed herein, or with other methods and devices known in the art. | 2012-07-12 |
20120179201 | Chiropractic spinal manipulation boards - A portable device that provides a stable rigid platform with two parallel peripheral elevations and a channel in between that can be applied to the spine or pelvis of a patient placed in either a supine, sitting, or standing position, which the doctor uses to obtain therapeutic effects to correct spinal and pelvic disorders, conditions, and syndromes in conjunction with the application of manual manipulation and manipulative surgery beyond what can be done by using the hands alone. | 2012-07-12 |
20120179202 | CERVICAL PILLOW FOR TREATMENT OF CERVICAL SPINE DISEASES - A cervical pillow for treatment of cervical spine diseases includes a padded member made of resilient materials such as foam, rubber, or cotton. The padded member has a rectangular flat bottom side, vertically flat left and right sides, a rounded front side, a thin back side, and a wavy top side that has a flat portion connecting to the front side, a slightly concave portion in the middle, and a very convex portion connecting to the back side. The cervical pillow further includes a nearly rectangular solid block made of high-strength materials such as plastic or compressed rubber. This solid block is embedded within the padded member along its back side and under the very convex portion of its top side. | 2012-07-12 |
20120179203 | Chiropractic table apparatus and method of use - A chiropractic table has a base, a table support member connected to the base and extending upward from the base, an axial-lateral-tilt mechanism laterally connected to table support member, a cephalad section connected transversely to and being supported by the table support member above the base, a head section connected to and extending longitudinally from a first cephalad section end of the cephalad section, and a caudal section interconnected with the axial-lateral-tilt mechanism and the table support member and being positioned longitudinally adjacent a second cephalad section end of the cephalad section where the axial-lateral-tilt mechanism has an axial pivot mechanism configured to axially swing the caudal section along a predefined arc, the arc coinciding with a predefined radial distance from a pivot axis that is parallel to a longitudinal axis of the chiropractic table and located a predefined distance above a top surface of the chiropractic table. | 2012-07-12 |
20120179204 | Transconnector - A transconnector for use in interconnecting a pair of longitudinal spinal rods in a spinal fixation procedure. The transconnector includes a bridge member and first and second spinal rod engaging members. The bridge member may include first and second members, wherein the first and second members are moveably associated with one another so that the distance between the first and second spinal rod engaging members can be adjusted. The first and second spinal rod engaging members include a rod receiving channel for receiving one of the spinal rods therein. The spinal rod engaging members may be articulating in, for example, the yaw and roll positions or non-articulating with respect to the bridge members. The spinal rod engaging members preferably include a spring, for example, a spring washer, to provide an opposing force so that the spinal rod engaging members can provisionally snap onto the spinal rods. | 2012-07-12 |
20120179205 | CONNECTOR APPARATUS AND METHOD - A spinal stabilization apparatus and method according to which a fastener is engaged with a bone structure of a spinal system. The fastener is connected to a rod by moving the rod downward toward the fastener in a sagittal plane, and the direction of extension of at least a portion of the rod in a coronal plane may be selectively adjusted in predetermined angular increments through 360 degrees. | 2012-07-12 |
20120179206 | ANCHORING MEMBER WITH SAFETY RING - A method for osteosynthesis of a spinal column using an assembly including a bone anchor, a connector and a ring, the method comprising: inserting an anchoring part of the bone anchor into bone, the bone anchor including the anchoring part and a head, the head positioned to be in contact with the connector and ring; inserting a connecting member into the connector; and applying a force to the connecting member such that the connecting member applies the force against the ring and the bone anchor, wherein the head of the bone anchor contacts the connector, ring and connecting member during the application of the force. | 2012-07-12 |
20120179207 | SURGICAL PLATE SYSTEM AND METHOD - A surgical plate system, components and methods of using are described. A surgical plate system includes a plate having an anterior surface, a posterior surface, a longitudinal axis, a transverse axis and a through hole passing through the anterior and posterior surfaces. A variable fastener is configured and dimensioned to connect to the plate, the variable fastener having a head and a shaft extending distally from the head. The head is configured to assume different proximal end diameters. The head, in a first configuration allows inward flexing to reduce a diameter of the head to allow the head to pass through an entrance opening of the through hole. In a second configuration, the head is prevented from flexing inwardly thereby preventing the head from backing out of the entrance opening, while allowing articulation of the head, within the through hole, relative to the plate. | 2012-07-12 |
20120179208 | BONE PLATE SYSTEM FOR REPAIR OF PROXIMAL HUMERAL FRACTURE - A bone plate system for repair of a proximal humeral head fracture, which includes a fixation plate having a main body and a depending alignment flange, a plurality of elongated compression screws to extend through the intact humeral head into the cortical bone of the fractured portion and a cover plate. With the fixation plate in place, fastened to the humerus, the cover plate is in turn fastened to the fixation plate and provides a defined amount of clearance in a region adjacent the heads of the compression screws to allow measured back-out of the screws upon settling of the fractured bone portion at the fracture site. | 2012-07-12 |
20120179209 | RECEIVING PART FOR RECEIVING A ROD FOR COUPLING THE ROD TO A BONE ANCHORING ELEMENT AND A BONE ANCHORING DEVICE - A receiving part for coupling a rod to a bone anchoring element includes: a receiving part body with a rod receiving portion and a head receiving portion having an open end for introducing a head of a bone anchoring element, and a locking ring, wherein the head receiving portion includes a plurality of flexible wall portions, the flexible wall portions and the locking ring being configured to engage each other at circumferentially distinct pressure areas having positions corresponding to circumferentially separated projections on at least one of the flexible wall portions or the locking ring, and wherein the locking ring exerts a first force on at least one of the flexible wall portions at a corresponding pressure area, and exerts a second force less than the first force on the at least one flexible wall portion in a region circumferentially adjacent to the corresponding pressure area. | 2012-07-12 |
20120179210 | PEDICLE SCREW ASSEMBLY WITH INCLINED SURFACE SEAT - A bone stabilizer assembly includes a fixation element, a coupling element, and a compression nut. The fixation element is adapted to engage a bone and having a head portion and shank portion. The coupling element has an internal bore sized to receive the shank portion of the fixation element and a pyramid-shaped seat for supporting the head portion of the fixation element. The coupling element is adapted to receive a stabilizer rod. The compression nut is engagable with the coupling element and is adapted to rotatingly move distally into the coupling element to translate a force to the head portion through the rod and the saddle such that the head portion is forced against the seat of the coupling element to prevent relative movement between the fixation element and the coupling element. | 2012-07-12 |
20120179211 | RECEIVING PART FOR RECEIVING A ROD FOR COUPLING THE ROD TO A BONE ANCHORING ELEMENT AND BONE ANCHORING DEVICE WITH SUCH A RECEIVING PART - A receiving part for coupling a rod to a bone anchoring element includes a receiving part body including a head receiving portion having an open end and a first exterior surface portion, the head receiving portion being flexible to allow introduction and clamping of a head of a bone anchoring element, and a locking ring having a first interior surface portion configured to engage the first exterior surface portion of the head receiving portion in a first contact region to lock an angular position of the head, wherein the first interior surface portion is spaced apart from an end of the locking ring, and wherein one of the first exterior surface portion or the first interior surface portion includes a cylindrical surface, and the other one of the first exterior surface portion or the first interior surface portion includes another cylindrical surface or a ring-shaped bulge portion. | 2012-07-12 |
20120179212 | Polyaxial bone anchor with compound articulation and pop-on shank - A polyaxial bone screw assembly includes a threaded shank body having an integral shank head receivable in a one-piece receiver having an upper channel for receiving a longitudinal connecting member and a lower cavity cooperating with a lower opening. A compression insert (some with an independent tool lock, lock and release feature and/or friction fit feature) and a split retaining ring articulatable with respect to both the shank head and the receiver (prior to locking) cooperate with the receiver to provide for pop- or snap-on assembly of the shank with the receiver either prior to or after implantation of the shank into a vertebra. | 2012-07-12 |
20120179213 | Method And Apparatus For Facilitating Navigation Of An Implant - The present invention describes a targeting system suitable for guiding a biocompatible device to a target area within the body (in vivo) and method of using the same. The system includes a targeting member that is attached to the biocompatible device and may optionally include a steering material. The system includes a passer element located at the distal end of a wand. The wand includes a trigger like member adjacent a hand grip. Actuation of the trigger like member will result in a pivotal movement of the passer element that positions the targeting member such that the connected biocompatible device is positionable relative to the target area. | 2012-07-12 |
20120179214 | System for Pushing and Pulling Surgical Implants into Position in Vivo Via a Tether - The present invention describes a system suitable for guiding a biocompatible device to a target area within the body (in vivo) and method of using the same. The system includes a targeting member being constructed of, or having a steering material, which can be coupled to a biocompatible device. The system further includes one or more devices which are used to maneuver the targeting member into position prior to attachment of the biocompatible device. The biocompatible device is traversed into position through the passageway created by the targeting member and secured to one or more anchoring members. | 2012-07-12 |
20120179215 | INTRACORPOREAL DEVICE FOR MOVING TISSUE - A device for moving tissue inside the body, in particular bone tissue, may include a reference part, a transport part which is slidably mounted relative to the reference part; a threaded rod pivotably mounted relative to the reference part, a control shaft, driving means connecting the control shaft to the threaded rod, a connecting nut between the transport part and the threaded rod, the connecting nut being mounted onto the threaded rod and being rotatably guided relative to the reference part, and means for converting the movement of the connecting nut along the threaded rod into a movement of the transport part relative to the reference part. In order to limit the longitudinal translation of said threaded rod relative to the reference part, a first abutment and a second abutment rigidly connected to the threaded rod respectively cooperate with a first bearing and a second bearing, these bearings being rigidly connected to the reference part and being placed at a distance from one another between the abutments. The connecting nut is movable along the threaded rod between the first bearing and second bearing. | 2012-07-12 |
20120179216 | NEURAL STIMULATION SYSTEM FOR CARDIAC FAT PADS - Various aspects relate to a device which, in various embodiments, comprises a header, a neural stimulator, a detector and a controller. The header includes at least one port to connect to at least one lead, and includes first and second channels for use to provide neural stimulation to first and second neural stimulation sites for a heart. The controller is connected to the detector and the neural stimulator to selectively deliver a therapy based on the feedback signal. A first therapy signal is delivered to the first neural stimulation site to selectively control contractility and a second therapy signal is delivered to the second neural stimulation site to selectively control one of a sinus rate and an AV conduction. Other aspects and embodiments are provided herein. | 2012-07-12 |
20120179217 | Planar Anode for Use in a Wet Electrolytic Capacitor - A relatively thin planar anode for use in a wet electrolytic capacitor is provided. Through a combination of specific materials and processing techniques, the present inventors have surprisingly discovered that the resulting anode may possess a high volumetric efficiency, and yet still be able to operate at a high voltage and capacitance, thus resulting in a capacitor with a high energy density. More particularly, the anode is a pressed pellet formed from an electrically conductive powder that contains a plurality of particles (including agglomerates thereof). The particles may have a flake-like morphology in that they possess a relatively flat or platelet shape. The present inventors have discovered that such a particle morphology can optimize packing density, and thus reduce the thickness of the anode and improve volumetric efficiency. Such particles can also provide a short transmission line between the outer surface and interior of the anode and also provide a highly continuous and dense wire-to-anode connection with high conductivity. Among other things, this may help increase the specific charge of the anode when anodized at higher voltages, thereby increasing energy density. The particles may also increase the breakdown voltage (voltage at which the capacitor fails) and help lower equivalent series resistance (“ESR”). | 2012-07-12 |
20120179218 | DEFIBRILLATOR HAVING SPECIALIZED OUTPUT WAVEFORMS - An output stage for use in a therapeutic defibrillator enables practical use of specialized output waveforms optimized for cardiac defibrillation. A pulse-width modulated (PWM) switching amplifier, connected to a high voltage source capacitor and to one or more output bridges corresponding to different electrode placements, is adapted to operate with high efficiency, demonstrated at about 80%. The amplifier is capable of delivering a defibrillating electric shock to a heart in the form of a time-varying output voltage waveform of arbitrary shape. Efficiency improvement is accomplished through the use of a high voltage reservoir capacitor network configured to minimize a voltage differential between the high voltage reservoir and the output voltage. The switching amplifier features both step-up and step-down amplifier capability. A PWM control unit is positioned within the circuit so as to reduce complexity by eliminating a need for additional isolation circuitry. | 2012-07-12 |
20120179219 | STIMULATION SYSTEM, IN PARTICULAR A CARDIAC PACEMAKER - A stimulation system, an implantable electrode device and a method for operating an implantable electrode device are proposed. A simplified implantation, a simple construction and reliable control are made possible by the electrode device being supplied with energy, and controlled, in an exclusively wireless manner via a time-variable magnetic field. The magnetic field is generated by an implanted control device. | 2012-07-12 |
20120179220 | METHODS AND SYSTEMS FOR DETERMINING IF AN ARRHYTHMIA INITIATED IN AN ATRIUM OR A VENTRICLE - Validated atrial and/or ventricular interval decreases are used to discriminate between VT and SVT. Atrial and/or ventricular intervals are monitored in order to detect decreases in such intervals (which are indicative in increases in rate). The atrial intervals can be, e.g., AA intervals, and the ventricular intervals can be, e.g., VV intervals. A detected atrial and/or ventricular interval decrease can be a decrease that is greater than an interval decrease threshold. Detected atrial and/or ventricular interval decreases can be validated by examining atrial and/or ventricular intervals before and after a detected atrial and/or ventricular interval decrease. The use of the validated atrial and/or ventricular interval decreases to classify an arrhythmia as SVT or VT can be called arrhythmia initiation analysis, since it is believed to determine whether the initiation of the arrhythmia is in an atrium or a ventricle. | 2012-07-12 |
20120179221 | BUNDLE OF HIS STIMULATION SYSTEM - A system for therapeutically stimulating a His bundle includes an implantable pulse generator and a multi-polar medical electrical lead. The generator is configured for subcutaneous implantation and to generate a pacing stimulus. The lead includes a connector assembly, a flexible tubular body, a distal tip assembly and coil conductors. The body extends intravascularly from the generator to a location proximate the His bundle and includes a proximal end, a distal end, and a longitudinal lumen. The tip assembly includes an electrode, a fixation helix, and a shank portion. The helix extends to a location proximate the His bundle and is operable as an electrically isolated electrode. The shank portion extends within the lumen and includes a receptacle for receiving a stylet tip. The conductors extend longitudinally through the lumen and are coupled to the electrode and the helix. One or both of the conductors defines a stylet lumen. | 2012-07-12 |
20120179222 | SYSTEM AND METHOD FOR AVOIDING, REVERSING, AND MANAGING NEUROLOGICAL ACCOMMODATION TO ELECTRICAL STIMULATION - A method of operating a neurostimulation device comprises varying a first stimulation parameter under user control while fixing a second stimulation parameter, generating a plurality of stimulation parameter sets from the varied first stimulation parameter and the fixed second stimulation parameter, outputting a pulsed electrical waveform from the neurostimulation device between electrodes in accordance with the stimulation parameter sets, such that a therapeutic effect is achieved while allowing neural tissue to undergo neurological accommodation, changing the second stimulation parameter, varying the first stimulation parameter under user control while fixing the second changed stimulation parameter, generating another plurality of stimulation parameter sets from the varied first stimulation parameter and the fixed changed second stimulation parameter, and outputting the pulsed electrical waveform from the neurostimulation device between the electrodes in accordance with the other stimulation parameter sets to maintain the therapeutic effect while the neural tissue is neurologically accommodated. | 2012-07-12 |
20120179223 | METHODS AND SYSTEMS OF COMPENSATING FOR A DISABLED ELECTRODE - An exemplary method includes 1) identifying, by a cochlear implant system, an electrode included within an array of electrodes as being a disabled electrode, 2) selecting, by the cochlear implant system, at least two non-adjacent electrodes surrounding the disabled electrode, and 3) simultaneously applying, by the cochlear implant system, stimulation current to the at least two non-adjacent electrodes to compensate for a loss of stimulation resulting from the disabled electrode. Corresponding methods and systems are also disclosed. | 2012-07-12 |
20120179224 | COMPENSATION CURRENT OPTIMIZATION FOR COCHLEAR IMPLANT SYSTEMS - An exemplary method includes 1) applying a main current to a first electrode disposed within a patient and associated with a first pitch, 2) concurrently applying a compensation current to a second electrode disposed within the patient and associated with a second pitch during the application of the main current, the compensation current being out-of-phase with the main current, and 3) optimizing an amount of the compensation current to result in a target pitch being presented to the patient that is distanced from the first pitch in a pitch direction opposite a pitch direction of the second pitch in relation to the first pitch. Corresponding methods and systems are also disclosed. | 2012-07-12 |
20120179226 | Therapeutic and Safety Grip Device - A grip device for use in one's hand includes a compressible member of a size to fit within one's hand and capable of being squeezed by the hand and a thermal element operably connected to the compressible member which is equipped for generating a non-ambient temperature for a sustained period during such period said device remains compressible. A sensor and transmitter circuitry is connected to the compressible member which when the grip device is compressed sends a signal indicative that compression is taking place. A computer with software receives and displays the signal to a recipient. | 2012-07-12 |
20120179227 | Reduction of Pain through Lower Fluence Rates and Longer treatment Times - A method of treating a subcutaneous fat region is provided. The method includes generating electromagnetic radiation having a wavelength of about 1,200 nm to about 1,230 nm and delivering an average power density of less than or equal to about 2.3 W/cm | 2012-07-12 |
20120179228 | APPLICATIONS OF THE STIMULATION OF NEURAL TISSUE USING LIGHT - The present invention comprises systems and methods for stimulating target tissue comprising a light source; an implantable light conducting lead coupled to said light source; and an implantable light-emitter. The light source, lead and emitter are used to provide a light stimulation to a target tissue | 2012-07-12 |
20120179229 | Laser System for Non Ablative Treatment of Mucosa Tissue - A laser system has a laser source for generating a laser beam, a control unit, and a hand piece for manually guiding the laser beam onto a target area. A wavelength (λ) of the laser beam is in a range from above 1.9 μm to 11.0 μm inclusive. The laser system is adapted for a thermal, non ablative treatment of mucosa tissue by the laser beam such, that the laser source generates the laser beam in single pulses with a pulse duration (t | 2012-07-12 |
20120179230 | Device For Performing Beauty, Physiotherapy and Hydrotherapy Treatment - The invention is a device capable of performing an unspecified number of treatments on any part of the body, locally or generally and at high speed, wherein the patient does not come into contact with vapours or fluids, whether in manual or automatic operating mode with pre-programmed treatments, using to this end contrasting applications as an essential base. The patient receives the contrasting applications through so-called contrast modules ( | 2012-07-12 |
20120179231 | THERMAL TREATMENT SYSTEM AND APARATUS WITH BIOFEEDBACK-DRIVEN PROTOCOL - The invention provides for a thermal treatment device for generating a feedback-driven protocol for thermal treatment of a human or animal body part. The device has measurement means adapted to acquire data of a thermal treatment from the body part and means for adapting the thermal treatment of the body part on the basis of the data acquired. Further, a method for generating a feedback-driven protocol for thermal treatment of a human or animal body part is provided. The method comprises the steps of acquiring data of a thermal treatment from the body part and adapting the thermal treatment of the body part on the basis of the data acquired. | 2012-07-12 |
20120179232 | HEATING DEVICE - An object of the invention is to provide a heating device that can warm the body to promote blood circulation, while restricting the movement of an area of the body to which the heating device is applied. | 2012-07-12 |
20120179233 | RF REJECTING LEAD - A lead assembly for an implantable medical device includes a lead body having a first portion and a second portion. The first portion adapted for coupling to a pulse generator and the second portion is adapted for implantation. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils each including a plurality of turns. Two or more adjacently wound consecutive turns of the first conductive coil alternate with two or more adjacently wound consecutive turns of the second conductive coil. | 2012-07-12 |
20120179234 | DEFIBRILLATOR WITH PRE-CONNECTED ELECTRODE PADS WITH REDUCED SUSCEPTIBILITY TO FALSE ASYSTOLE INDICATIONS - A defibrillator electrode set for a defibrillator which senses the capacitance of an attached electrode set includes an electrode set coupled to the defibrillator by an adapter cable. The adapter cable and electrode set are pre-connected to the defibrillator prior to use. The electrodes are stored in a sealed foil package to retard gel desiccation prior to use. To reduce the capacitance of the electrode set seen by the defibrillator, the capacitance between the stored electrodes and the foil package is reduced by using a thicker dielectric layer for the layer of an electrode which opposes a wall of the foil package. In a constructed embodiment, one sixteenth inch thick polyethylene foam is used for the electrode layer opposing the wall of the foil package. | 2012-07-12 |
20120179235 | COMPOSITE STENT GRAFTS FOR IN SITU ASSEMBLY AND RELATED METHODS - Composite stent grafts can include separate components that are capable of being repositioned relative to each other in situ. In some examples, a stent and a graft that are attached to each other in an insertion package do not overlap each other. The graft and stent are moved relative to each other in situ. | 2012-07-12 |
20120179236 | SIDEPORT ENGAGEMENT AND SEALING MECHANISM FOR ENDOLUMINAL STENT-GRAFTS - An endovascular prosthesis ( | 2012-07-12 |
20120179237 | SPRAY SYSTEM AND METHOD OF MAKING PHASE SEPARATED POLYMER MEMBRANE STRUCTURES - A spray system and method of using such spray system to fabricate a polymer membrane structure for use as a vascular graft or tissue engineered scaffold is provided. Generally, this spray system includes the use of at least two spray apparatus to apply different polymer and solvent mixtures to the outer surface of a mandrel to form a blended layer. Upon curing of the blended layer, phase separation occurs leading to the formation of a polymer membrane structure having variable properties along at least a portion of its longitudinal axis. | 2012-07-12 |
20120179238 | STENT HAVING VARIABLE STIFFNESS - A plurality of radially expandable cylindrical elements are generally aligned along a common longitudinal axis and are interconnected by a plurality of interconnecting members placed so that the stent is flexible in the longitudinal direction. The plurality of cylindrical elements collectively form first and second stent ends longitudinally separated by a stent body. At least one of the first and second stent ends is reverse-tapered laterally outward from the longitudinal axis and longitudinally away from the stent body. The stent body has a stiffness value of X, and at least one of the first and second stent ends has a stiffness value of Z, with Z being greater than | 2012-07-12 |
20120179239 | VASCULAR PROSTHESIS CONNECTING STENT - An expandable vascular stent includes an m 3 n array of ovals formed in a cylinder, m being the number of columns of ovals in the circumferential direction and n being the number of rows of ovals in the axial direction, and a plurality of prongs extending inwardly from the outer ends of respective ovals in rows 1 and n of the m 3 n array, and being arranged in facing pairs extending from axially-aligned ovals. The cylinder is expandable from an initial diameter to a pre-determined final diameter, wherein an increase in the diameter of the stent results in a substantial decrease in the length of the stent. The tube and the prongs can be made of surgical stainless steel, the tube being expandable using an angioplasty balloon; or the tube and the prongs can be made of a memory metal and the tube is self-expanding. | 2012-07-12 |
20120179240 | STENT/FIBER STRUCTURAL COMBINATIONS - A plurality of endoluminal segments axially connected by fiber bridges is disclosed. The endoluminal segments may be superelastic nitinol that is balloon-expandable or self-expanding. The intraluminal segments may possess a textured surface or at least one geometric feature per segment, located at the apex of a strut pair comprising the intraluminal segment, serving as an anchoring point for the fiber bridges. These geometric features may transmit axially compressive loads during deployment from a device such as a catheter, and may be capable of interlocking the endoluminal segments when constrained within a device such as a catheter. The fibers comprising the bridges may be polymeric, silk, collagen, bioabsorbable, or a blend thereof. The fiber network comprising the bridges may be regularly oriented, randomly oriented, localized, or continuous. The intraluminal segments and fiber bridges may be individually impregnated with therapeutic material, or may both be impregnated with therapeutic material. | 2012-07-12 |
20120179241 | STENT SEGMENTS AXIALLY CONNECTED BY THIN FILM - In accordance with the present invention, there is provided a stent for insertion into a vessel of a patient. The stent has a front and back open ends and a longitudinal axis extending therebetween. The stent has a plurality of adjacent hoops that are held in alignment with the longitudinal axis between the front and back open ends by a thin film tube. The hoops are attached to either the inner or outer surface of the thin film tube. The stent is compressed into a first smaller diameter for insertion into the vessel with a delivery tube and a second larger diameter for deployment into the vessel. The inventive stent can be retracted into the delivery tube if it is improperly deployed. | 2012-07-12 |
20120179242 | IMPLANTABLE ARTICLE, METHOD OF FORMING SAME AND METHOD FOR REDUCING THROMBOGENICITY - Endothelialization of a bodily fluid or tissue-contacting, particularly blood-contacting, surface may be accomplished to render that surface substantially non-thrombogenic. Thrombosis may also be mitigated or eliminated by providing an eroding layer on the surface that results in the removal of any thrombus formation as the layer erodes. An implantable device may utilize at least one surface having a plurality of nano-craters thereon that enhance or promote endothelialization. Additionally, an implantable device may have at least one first degradable layer for contacting bodily fluid or tissue and disposed about a central core, and at least one second degradable layer between the first degradable layer and the central core. The first degradable layer has a first degradation rate and the second degradable layer has a second degradation rate which degrades more slowly than the first degradable layer on contact with bodily fluid or tissue. | 2012-07-12 |
20120179243 | METHODS AND APPARATUSES FOR DEPLOYING MINIMALLY-INVASIVE HEART VALVES - A method for replacing native valve function of a diseased aortic valve in a patient is provided. The method comprises: (a) guiding a catheter system having a balloon through the vasculature of the patient; (b) guiding an artificial heart valve assembly through the vasculature of the patient; (c) while the catheter system is in the patient's vasculature, positioning the artificial heart valve assembly about the balloon of the catheter system; (d) delivering the artificial heart valve assembly to the region of the diseased aortic valve; (e) while the patient's heart is beating, expanding the artificial heart valve assembly in the region of the diseased aortic valve; and (f) withdrawing the catheter system from the patient's vasculature. | 2012-07-12 |
20120179244 | Device and System for Transcatheter Mitral Valve Replacement - This invention relates to the design and function of a compressible valve replacement prosthesis which can be deployed into a beating heart without extracorporeal circulation using a transcatheter delivery system. The design as discussed focuses on the deployment of a device via a minimally invasive fashion and by way of example considers a minimally invasive surgical procedure preferably utilizing the intercostal or subxyphoid space for valve introduction. In order to accomplish this, the valve is formed in such a manner that it can be compressed to fit within a delivery system and secondarily ejected from the delivery system into the annulus of a target valve such as a mitral valve or tricuspid valve. | 2012-07-12 |
20120179245 | METHODS OF ASSEMBLING AND DELIVERING AN ANNULOPLASTY RING - A holder for an annuloplasty ring having a template defining a proximal face opposite the distal face, and a peripheral edge about which the annuloplasty ring conforms. The annuloplasty ring anchors to the template using one or more flexible filaments. The template includes a single cutting well on its proximal face over which the flexible filament is suspended. Desirably, the single cutting well is located adjacent the peripheral edge so as to be away from any handle connections for ease of access. The flexible filament emerges above the proximal face of the template at only one location at the cutting well, thus presenting a one cut quick-release structure that is highly visible to the surgeon. | 2012-07-12 |
20120179246 | MITRAL VALVE CERCLARGE ANNULOPLASTY APPRATUS AND METHOD THEREOF - A mitral cerclage annuloplasty apparatus comprises a tissue protective device and a cap device having a cerclage suture disposed within a first protective tube and a second protective tube, the proximal portions of the two tubes being attached side-by-side longitudinally to define a stem portion, the distal portions of the two tubes being separated thereafter, and a cap device that covers the stem portion wherein the stem portion and the cap device interlock, so that once the cerclage suture is knotted on the outer surface of the cap device, cap device can be pulled outwardly to enhance and maintain tension applied to the mitral annulus thus successfully treating the mitral regurgitation. | 2012-07-12 |
20120179247 | APPARATUS AND METHOD FOR TREATING A REGURGITANT HEART VALVE - An apparatus is provided for treating regurgitation of blood flow through a diseased heart valve. The diseased heart valve includes an annulus, anterior and posterior valve leaflets, and a subvalvular apparatus. The apparatus includes a substantially annular support member and at least one infra-annular support member securely connected thereto. The substantially annular support member has at least a first intermediate portion, a second intermediate portion, and a posterior end portion extending between the first and second intermediate portions. The posterior end portion is dimensioned for attachment to a posterior portion of the annulus of the diseased heart valve. The at least one infra-annular support member is securely connected to the substantially annular support member at a first location. The at least one infra-annular support member is dimensioned to extend below at least one of the posterior and anterior valve leaflets and across or behind at least one subvalvular structure. | 2012-07-12 |
20120179248 | VISION PROSTHESIS WITH ARTIFICIAL MUSCLE ACTUATOR - A visual prosthesis includes an artificial muscle configured to deform in response to a focusing signal. The artificial muscle is coupled to at least a portion of an optical system for changing a focal point thereof. | 2012-07-12 |
20120179249 | ACCOMMODATING INTRAOCULAR LENS AND METHODS OF USE - The present invention relates to an accommodating intraocular lens, which is suitable for replacement of the natural crystalline lens of the eye within the capsular bag. The intraocular lens can include a retainer plate with an annular region surrounding a central opening, and an optical lens. The retainer plate acts as a foundation for the optical lens, as the retainer plate can be positioned near or at the posterior portion of the lens capsule. The optical lens can sit on the retainer plate, but is otherwise not attached to the retainer plate. The optical lens can overlap or fit within the central opening of the retainer plate. The retainer plate can include a lip portion integrally disposed on a region of the retainer plate, wherein the lip provides a surface for holding at least a portion of an intraocular lens. | 2012-07-12 |
20120179250 | SYSTEM AND METHOD FOR BREAST AUGMENTATION - A system for cosmetic augmentation includes a plurality of microballoons. An injector can be provided for injecting microballoons into a subcutaneous pocket at a cosmetic site through an incision. A method for performing cosmetic augmentation surgery and microballoons for use in the method are also disclosed. | 2012-07-12 |
20120179251 | TISSUE MARKING IMPLANT - An implant for marking an area within a living body includes a matrix material and a marking material. The implant is formable to fit the shape and size of a cavity in the human body. The implant is configured to support tissue surrounding the cavity and to allow in-growth of fibrous tissue into and replace at least a portion of the matrix material. | 2012-07-12 |
20120179252 | PROSTHETIC DEVICE AND METHOD OF MANUFACTURING THE SAME - A knitted prosthetic device has at least two knitted sections, where each knitted section has at least one row of fiber. The knitted prosthetic device also has at least one intra-articular section disposed between the at least two knitted sections. In addition, the at least one intra-articular section has at least one single continuous fiber traversing the at least one intra-articular section and the at least two knitted sections, where the at least one single continuous fiber forms a plurality of traverses extending between the at least two knitted sections. In particular, embodiments may be used as ligament prostheses by anchoring each of the at least two knitted sections to a bone section of a patient. Such embodiments may be constructed from a strong polymer, preferably, but not limited to, silk, where the polymer provides ligament support but bioresorbs as load bearing responsibilities are transferred to tissue resulting from ingrowth. | 2012-07-12 |
20120179253 | PROSTHETIC DEVICE AND METHOD OF MANUFACTURING THE SAME - A knitted prosthetic device has at least two knitted sections, where each knitted section has at least one row of fiber. The knitted prosthetic device also has at least one intra-articular section disposed between the at least two knitted sections. In addition, the at least one intra-articular section has at least one single continuous fiber traversing the at least one intra-articular section and the at least two knitted sections, where the at least one single continuous fiber forms a plurality of traverses extending between the at least two knitted sections. In particular, embodiments may be used as ligament prostheses by anchoring each of the at least two knitted sections to a bone section of a patient. Such embodiments may be constructed from a strong polymer, preferably, but not limited to, silk, where the polymer provides ligament support but bioresorbs as load bearing responsibilities are transferred to tissue resulting from ingrowth. | 2012-07-12 |
20120179254 | IMPLANT AND METHOD FOR REPAIR OF THE ANTERIOR CRUCIATE LIGAMENT - Described herein are methods and devices for use in repair of a patient's anterior cruciate ligament (ACL). These methods (and devices for performing them) allow the repair, rather than merely replacement, of the ACL. For example, described herein are anchoring devices that may be inserted into a bone and may anchor a scaffolding/support (e.g., graft) material within the bone so that the torn or damaged end of the ACL may be secured to the scaffolding/support material within the femoral notch. These anchoring devices and method of using them are particularly well suited for use with the continuous suture passers described herein, since these suture passers may allow access to previously inaccessible regions of the knee (or other body regions). | 2012-07-12 |
20120179255 | EXPANDABLE SPINAL IMPLANT DEVICE - An expandable spinal implant device for supporting vertebral bodies can include first and second body members and first and second expansion mechanisms. The body members can each have a first end positionable toward one of the vertebral bodies and can each define a hollow interior. The expansion mechanisms can be spaced apart from each other and can include a first drive shaft and a second drive shaft, respectively. The first and second drive shafts can each have a gear member fixedly coupled thereto. Each drive shaft can be threadably engaged at a first side to the first body member and at a second side to the second body member. The expansion mechanisms can be operable to effect axial displacement of the first body member relative to the second body member by rotationally driving the gear members of the first and second drive shafts. | 2012-07-12 |
20120179256 | Facet Arthroplasty Devices and Methods - Devices and surgical methods treat various types of adult spinal pathologies, such as degenerative spondylolisthesis, spinal stenosis, degenerative lumbar scoliosis, and kypho-scoliosis. Various types of spinal joint replacement prostheses, surgical procedures for performing spinal joint replacements, and surgical instruments are used to perform the surgical procedures. | 2012-07-12 |
20120179257 | Expansion band with unilateral strain and manufacturing method thereof - An expansion band includes a first layer, a second layer, a shrinking layer for shrinking said first layer and said second layer, a bond line for sealing said first layer and said second layer to form an inner space therein and dividing said inner space into a plurality of air passages which can communicate with each other, a plurality of air passages formed between said first layer and said second layer, and an air nozzle communicate with said air passage. | 2012-07-12 |
20120179258 | SPINAL SPACER DEVICES, TOOLS, AND METHODS - A spacer device for spinal fixation, such as in corpectomies and discectomies, includes a core and two end plates mounted to the core. One end plate is mounted to each respective end of the core. The core can be configured and adapted to be adjustable to allow for contraction and/or distraction of the end plates. The end plates can include apertures therethrough to facilitate osseointegration of the spacer device within a patient's spine. The angle of the endplates can each be adjusted with respect to the core of the spacer device, for example to accommodate lordosis. A containment mesh is included around the spacer device, wrapping circumferentially around the end plates, and spanning from end plate to end plate. The containment mesh defines a containment volume between the end plates for containing bone replacement materials such as allograft or man-made materials. | 2012-07-12 |
20120179259 | INTERVERTEBRAL IMPLANTS, SYSTEMS, AND METHODS OF USE - An intervertebral implant frame that is configured to be attached to a spacer body can include a pair of arms that extend longitudinally from a support member such that the arms extend substantially around the spacer body. The arms may be configured to expand, crimp, or otherwise engage the spacer body to thereby hold the spacer body to the frame. The spacer body may be made from bone graft. | 2012-07-12 |
20120179260 | SPINAL IMPLANT SYSTEM AND METHOD - A spinal implant system is disclosed. The system disclosed has a first footing adapted for inter-vertebral contact with a first vertebral body, a second footing adapted for inter-vertebral contact with a second vertebral body adjacent to the first vertebral body; and, a support slideably insertable between said first footing and said second footing while said first and second footings are in-situ between said first and second vertebral bodies. The footings provide a path for the support. Distractor instruments are disclosed. Methods of use, in surgery, are also disclosed. | 2012-07-12 |
20120179261 | INTERBODY SPACER - An interbody spacer includes a connecting portion and a pair of leg portions extending from the connecting portion. The connecting portion and the pair of leg portions define top and bottom surfaces configured and adapted to engage first and second vertebral bodies, respectively, and inner and outer sidewalls extending between the top and bottom surfaces. In particular, the top and bottom surfaces of the leg portions include first projections defining a first angle with the respective top and bottom surfaces of the leg portions. The top and bottom surfaces of the connecting portion include second projections defining a second angle with the respective top and bottom surfaces of the connecting portion. The first and second angles are different. | 2012-07-12 |
20120179262 | HUMERAL COMPONENT OF A SHOULDER PROSTHESIS AND METHODS OF SHOULDER ARTHROPLASTY - A humeral component of a shoulder prosthesis encloses a stem module which has a shank and an upper shank portion with a stem support surface. A joint adapter is adapted to hold either a liner or a spherical cap. The joint adapter has an adapter support surface which interfaces with the stem support surface. Further, the stem support surface and the adapter support surface have corresponding radial arc shaped sections which allow positioning of the joint adapter against the stem module at different inclination angles. For fastening the joint adapter to the stem module, a bolt or screw is provided. | 2012-07-12 |
20120179263 | STEMLESS SHOULDER IMPLANT - A humerus implant for a reverse shoulder prosthesis has a cup shaped body and a thread at the outside of the body. The thread has a plurality of fins with cut-outs between the fins. At least one fin has an inclined leading surface which helps in incising into the bone by rotating the body in an inward direction. Furthermore, at least one fin has a forward oriented undercut trailing surface blocking rotation in the outward direction. | 2012-07-12 |
20120179264 | PROSTHETIC PATELLA - A system of prosthetic patellar components including first and second prosthetic patellar components having dissimilar perimeter shapes and which are interchangeably usable without altering the securement feature formed on the natural patella or the position of the apex of the articulating surface of the prosthetic patella is described. A keyed securement feature as well as a patellar implant having a single offset mounting post for facilitating the proper placement of a patellar prosthesis on a natural patella based on patella tracking are also described. | 2012-07-12 |
20120179265 | KNEE PROSTHESIS - A knee prosthesis for a knee joint with a medial ball-like femoral condyle and with a width “w” is characterized on the lateral compartment by:—a trace-line “Lt | 2012-07-12 |
20120179266 | BICRUCIATE RETAINING TIBIAL BASEPLATE DESIGN AND METHOD OF IMPLANTATION - A base component for a tibial implant has a lateral compartment and a medial compartment spaced from the lateral compartment defining an open central section therebetween. A connecting portion connects the medial and lateral compartments at an anterior end of the base component which anterior end is located adjacent the anterior tibia. The open central section of the base component intermediate the spaced medial and lateral compartments is open to a posterior end of the base component. The medial and lateral compartments have a bone contacting surface and a superiorly facing surface. The connecting portion has a curved anteriorly facing surface and has a first angled surface extending at an angle from adjacent the anterior end of the base component at a bone contacting surface of the connecting portion superiorly to a posterior end of the connecting portion. The first angled surface defining an anterior end of the open central section. | 2012-07-12 |
20120179267 | TRAPEZIUM IMPLANT FOR THUMB AND METHOD - An implant for the trapezium of the thumb carpometacarpal (CMC) joint comprising an integral elastomeric member configured to include a body portion having a tapered neck, having extending from one end thereof an elongated, longitudinally extending tapered portion adapted to be embedded into a reamed out-channel in the thumb metacarpal bone. After implantation, in the preferred embodiment of the method according to the invention, a segment of a nearby tendon, for example, the APL or FCR tendons, may be wrapped around the tapered neck of the implant to secure it in position, thereby forming a reinforced structure to inhibit dislocation of the prosthesis. However, in other methods, various other securing elements, including, but not limited to acellular matrices, may be used to retain the implant in position. | 2012-07-12 |
20120179268 | Metatarsal Implant - The present invention comprises a metatarsal head implant comprising a generally convex, hollow portion that fits over the metatarsal head of the great toe, a serrated stem, and one or more locking screws. The implant of the present invention may work in conjunction with either the patient's existing phalanx or one-piece phalanx implants designed and/or manufactured independently from the metatarsal implant. | 2012-07-12 |
20120179269 | CONSTRAINED ACETABULAR TRIALING SYSTEM - A trial head and shell for use in trial reduction of hip implants, and particularly bipolar implants, having locking features that prevent the head from dissociating from the shell during trialing, yet which allow the head and shell to be readily assembled and disassembled in the operating room. A cut-out region is formed in an outer bearing surface of the head. The cut-out region allows the head to pass through a trial shell opening and into the shell, yet is oriented such that when the head is associated with a femoral neck, the head cannot disassociate from the shell. Orientation indicators can be provided for use in assembly and disassembly. The trial head and associated shells can be provided in the form of a surgical kit including hip implants. Methods of use are provided. | 2012-07-12 |
20120179270 | LOW STRESS MULTIPLE FIXATION ACETABULAR COMPONENT - The disclosure relates to revision hip surgery or total hip arthroplasty situations in which it is difficult for a surgeon to secure or fix an acetabular cup or shell to the bone due, for whatever reason, to bone loss or other bone deficiency. The system may comprise a plurality of fasteners and an acetabular cup or shell having a plurality of openings to thereby allow the plurality of fasteners to be inserted at diverging angles to create multiple fixation points to distribute load and secure the shell to available bone. The system may also include a bearing insert for receiving a femoral head component and a plurality of spacers for creating a cement mantle. | 2012-07-12 |
20120179271 | Devices and Methods for Tissue Engineering - A tissue engineering scaffold of interconnected and bonded fiber having a property with a value that is spatially distributed in at least two regions is provided. The scaffold has at least two regions with properties, such as porosity, strength, elastic modulus, osteoconductivity, and bioactivity that can be controlled and modified through fabrication processes that alter the pore size, pore size distribution, composition, and bonding of fiber and other additives. The value of the property can be provided with a gradient between each of the adjacent spatially distributed regions. | 2012-07-12 |
20120179272 | Braided Prosthetic Sockets with Attachment Plates and Methods of Manufacture - This invention provides new above knee (AK) and below the knee (BK) prosthetic sockets and implements specific manufacturing processes for the production of prosthetic sockets through the automated, computer controlled bi-axial and tri-axial braiding of sockets, over a mold or mandrel made of carved foam, plaster material or wax that is a replica of the patient's truncated limb, and is created by a Computer Aided Design (CAD) file controlling a Numerically Controlled (CNC) machine tool. This method of manufacture using aerospace fibers such as graphite or Kevlar, and high performance resins, is used to create a socket which is stronger and lighter weight than conventionally manufactured sockets. Braiding also allows incorporation of woven cloth, tapes and other reinforcements into the braiding process for added strength at selected areas. The method dramatically decreases the production time and cost of the prosthetic relative to conventional methods. | 2012-07-12 |
20120179273 | EXTRA-ARTICULAR IMPLANTABLE MECHANICAL ENERGY ABSORBING SYSTEMS AND IMPLANTATION METHOD - A system and method for sharing and absorbing energy between body parts. In one aspect, the method involves identifying link pivot locations, fixing base components and minimally invasive insertion techniques. In one particular aspect, the system facilitates absorbing energy between members forming a joint such as between articulating bones. | 2012-07-12 |
20120179274 | BIFURCATED, MULTI-PURPOSE PROSTHETIC FOOT - A prosthetic foot has a plurality of curvilinear leaf springs coupled to an attachment member, including a primary curvilinear leaf spring forming a forefoot arc, an elongated curvilinear leaf spring disposed below the forefoot arc, and a secondary curvilinear leaf spring forming a secondary forefoot member. The forefoot arc is laterally bifurcated while the forefoot reinforcement arc is laterally unitary. | 2012-07-12 |
20120179275 | Motion Control Systems - A system for allowing communication between a software application and at least one motion controller in a set of motion controllers comprising a set of selectable software modules, a software system, and a driver administrator. At least two selectable software modules expose a common software interface. The software application comprises at least one motion command associated with a primitive motion operation. The software system uses the driver administrator to select at least one selected software module and to load the selected software module. The software system commands at least one selected motion controller to perform the desired motion sequence using the plurality of motion commands of the software application and the common software interface. | 2012-07-12 |
20120179276 | SYSTEM AND METHOD FOR PROTECTION SYSTEM DESIGN SUPPORT - A method and system for examining, auditing, and safely evaluating process systems, including fluid pressure systems and nuclear plant systems, to aid overpressure design and/or sizing of overpressure equipment. The system includes a server subsystem, a storage subsystem, an assessment subsystem, and optionally a report generation subsystem, including computer hardware and application software for supporting these subsystems. | 2012-07-12 |
20120179277 | ATHLETIC RANKING SYSTEM - An athletic performance testing system comprises a controlled athletic performance testing environment, a host server for receiving athletic performance test data obtained using the controlled environment, and a website for displaying the athletic performance test data. The website includes a web page for displaying the rankings of the athletic performance test data. A method of ranking athletic performance test data comprises obtaining information about an athlete; setting up a controlled athletic performance testing environment; recording the athletic performance of the athlete performing under the controlled athletic performance testing environment; inputting the athletic performance test results of the athlete into a host server; and displaying and/or causing the athletic performance test results to be displayed on a website that automatically ranks the athletic performance test results. | 2012-07-12 |
20120179278 | Athletic Performance Sensing and/or Tracking Systems and Methods - Athletic performance sensing and/or tracking systems include components for measuring or sensing athletic performance data and/or for storing and/or displaying desired information associated with the athletic performance to the user (or others). Such systems can allow users a wide variety of options in creating workouts, selecting and presenting media content during the athletic performance, etc., e.g., to help keep users entertained and motivated. In some instances, user feedback may be used, optionally in combination with objective data relating to a workout, to control features of the workout routine, to control the music or other media content selected and/or presented, and/or to control features of future workout routines and/or the presented media content. | 2012-07-12 |
20120179279 | AUTOMATIC AUDIO CONFIGURATION BASED ON AN AUDIO OUTPUT DEVICE - Techniques are provided for determining, at an audio processing device, whether to produce high quality or low quality audio output based on one or more factors. The one or more factors may include the type of output device (e.g., headphones, built-in speakers, or USB audio devices) that is connected to the audio processing device and whether certain operations (e.g., mixing and/or scaling) are to be performed on the decoded audio content. Thus, the highest quality audio output is produced based on current conditions of the audio system, which includes the output device. If the current conditions of the audio system indicate that producing high quality audio output does not yield sufficient perceived benefits, then the audio processing device may produce lower quality audio output. | 2012-07-12 |
20120179280 | Pedestrian Warning System for an Electric or Hybrid Vehicle - A system is disclosed for warning at least one person in the vicinity of a motor vehicle, particularly an electric vehicle or a hybrid vehicle. The system includes at least one generator for generating an audio signal, a device for switching the generator on and off and/or for controlling the volume of the audio signal. At least one person and/or an object in the vicinity of the motor vehicle can be captured by a person-detecting system, and the at least one generator can be switched on and off and/or the volume of the audio signal can be controlled by the device as a function of the at least one person and/or the object. | 2012-07-12 |
20120179281 | SYSTEMS FOR DENTURE PREPARATION - Embodiments of the invention generally relate to systems and methods for designing and manufacturing dentures. More particularly, in certain embodiments, the invention relates to a system for preparing a denture base plate. The system includes a user interface and a design application for creating a virtual model, and a manufacturing apparatus for fabricating a denture base plate corresponding to the virtual model. In other embodiments, an apparatus is provided that includes a graphical interface and a design application for selecting a set of virtual denture teeth and placing and adjusting the virtual denture teeth in relation to each other and a virtual denture base plate. | 2012-07-12 |
20120179282 | System and Method for Semiconductor Device Fabrication Using Modeling - In one embodiment, a method of manufacturing a semiconductor device includes using a processor to generate a first three dimensional (3-D) resist profile for a first process condition using an layout mask of a target structure. The method further includes using a processor to generate a second 3-D resist profile for a second process condition using the layout mask. The first process condition includes a plurality of process variables, and the second process condition includes different values of the plurality of process variables than the first process condition. The method includes generating a 3-D process variable (PV) band profile by combining the first 3-D resist profile with the second 3-D resist profile and displaying a 3-D image of the 3-D PV band profile on a display. | 2012-07-12 |
20120179283 | MANAGING A PERFORMANCE OF SOLAR DEVICES THROUGHOUT AN END-TO-END MANUFACTURING PROCESS - The invention relates to managing performance of solar devices throughout a manufacturing process with multiple manufacturing steps. A method includes determining a plurality of key performance indicators for a solar device, determining a change behavior of each individual key performance indicator throughout manufacturing process steps, using a theoretical performance maximum of the solar device, comparing real performance of the solar device to the theoretical performance maximum, where the real performance is determined by key performance indicator changes throughout the entire manufacturing process resulting in a key performance indicator sensitivity matrix reflecting ultimate solar device performance, using the key performance indicator sensitivity matrix to improve each relevant manufacturing process step by modeling current manufacturing conditions to improve the key performance indicator, adapting the model in experimental manufacturing environment to match sensitivity curves between model and experiment, and using the model to calculate the performance of the solar devices. | 2012-07-12 |
20120179284 | Controller for Machine Tool - A controller for a machine tool has a program storage section in which an NC program is stored, a program analyzing section analyzing the NC program block by block in sequence and extracts operation commands for a feed mechanism, an execution control section executing the extracted operation commands and thereby controlling the feed mechanism, e program editing section changing the NC program, and a change information storage section in which change information relating to the changed portion of the NC program is stored. The execution control section, when executing the operation commands, checks whether the block of each operation command is the block immediately preceding a block relating to the changed portion, and when judging that it is the immediately preceding block, temporarily stops the operation of the feed mechanism before or after the execution of the operation command. | 2012-07-12 |
20120179285 | AUTOMATED REPAIR METHOD AND SYSTEM - A method and system for automated repair of a machine component is provided. According to the proposed method, a first geometry of the component, including a damaged portion of the component, is digitalized. A trough is then machined over the damaged portion of the component. The machining is numerically controlled using digitalized geometrical data of the first geometry of the component. A second geometry of the component is then digitalized subsequent to the machining, the second geometry including the trough. Subsequently, a material is deposited over the trough. The deposition of the material is numerically controlled digitalized geometrical data of the second geometry of the component. | 2012-07-12 |