31st week of 2014 patent applcation highlights part 57 |
Patent application number | Title | Published |
20140214087 | JOINT ALIGNER IMPLANT - A joint aligner ( | 2014-07-31 |
20140214088 | ORTHOPAEDIC PLATE - An orthopaedic device for repairing a portion of a body comprises an orthopaedic plate and a tissue protector. The orthopaedic plate is configured to attach to at least one bone. The tissue protector is securely attached to the orthopaedic plate and configured to at least partially detach from the orthopaedic plate after a force is applied to the tissue protector. The tissue protector includes a thinned region at a portion of the tissue protector proximate to the orthopaedic plate. A method of repairing parts of a body with an orthopaedic device having an orthopaedic plate and a tissue protector securely attached to the orthopaedic plate comprises placing the orthopaedic plate on at least one bone; fastening a fastener into the tissue protector and then the orthopaedic plate; and detaching the tissue protector from the orthopaedic plate after the fastener is completely fastened into the tissue protector and the orthopaedic plate. | 2014-07-31 |
20140214089 | DISTAL RADIUS VOLAR LOCKING PLATE WITH EXTENSION FOR ULNAR VOLAR FRAGMENT - A distal radius fixation plate for volar plating may comprise a distal radius fixation plate body configured to be placed adjacent a fractured volar distal radius and proximal to a watershed line of the volar distal radius and a distal radius fixation plate extension approximately 60 to 80% thinner on average than the distal radius fixation plate and projecting from the distal radius fixation plate body and configured to be placed so that it extends distal to the watershed line, the plate extension configured to curve around an ulnar/volar corner of the distal radius bone so as to engage the volar lip preferably without curving around other parts of the volar lip of the distal radius. The plate extension may have a hook at its upper end. The plate body may have an obliquely angled screw hole to buttress a radial styloid fragment. | 2014-07-31 |
20140214090 | BONE FIXATION SYSTEMS AND METHODS OF USE - A bone fixation system that may be configured to move at least one of a first bone segment and a second bone segment relative to the other, is disclosed. The system may include a first lever and a second lever pivotally coupled to the first lever. The first lever may include a first handle, a first jaw extending from the first handle, and an aperture extending through the first jaw. The aperture may be configured to receive a fixation element to thereby fixedly couple the first lever to a bone plate. The second lever may include a second handle, a second jaw extending from the second handle, and an aperture extending through the second jaw. The aperture may be configured to receive a temporary fixation element to operatively couple the second lever to the second bone segment. | 2014-07-31 |
20140214091 | Disposable Orthopedic Surgery Kit And Components - A disposable single indication orthopedic trauma surgical kit has no bone plates other than a single bone plate precountoured and sized to match an anatomic shape of a portion of a bone of a patient's extremity. The single bone plate has a plurality of fastener apertures. The surgical kit also has a plurality of fasteners with heads that are dimensioned to mate with the fastener apertures. The surgical kit also has a disposable torque driver adapted to engage the fastener heads. The foregoing components are contained in a sterile sealed container. | 2014-07-31 |
20140214092 | Bone Plate - A bone plate has a through-hole that extends from an upper side to a bone-side underside of the bone plate. A lip is formed in the through-hole, which lip projects from the lateral surface of the through-hole and extends in the circumferential direction of the through-hole. The lip extends over part of the circumference of the through-hole. In a circumferential section of at least 120° that lies opposite the lip, the lateral surface is free of a lip. Material is reshaped only to a lesser extent compared to a lip that extends over the entire circumference of the through-hole. The risk of complications occurring due to deposited particles is reduced. | 2014-07-31 |
20140214093 | Bone Plate and Plating System for Use of Same - A bone plate and plating system are for use of the same are disclosed. The bone plate includes a body having a span sufficient to overlap a portion of a bone. A screw hole extends through the body in order to receive a bone screw to attach for engaging the plate to the bone. The screw hole includes a counterbore having a beveled surface that intersects at a pinch point a bore having a conical surface of revolution that transitions into the bone engaging surface of the body. The beveled surface includes a variable geometry defining interleaved and rotationally-spaced contact and non-contact bone screw regions. | 2014-07-31 |
20140214094 | ANGULARLY STABLE FIXATION OF AN IMPLANT - A system and method of angularly stable fixation of an implant on a bone includes the steps of making at least one hole in the bone by means of a bone drill. An implant is placed on the bone in a desired position and joining the implant with the bone, such that the implant is prevented from rotation about its attachment point. A system is provided for use in the above described method. The system comprises a bone drill, an implant and a sonotrode for angularly stable fixation of the implant on the bone. The system can further comprise a joining element to join the implant with the bone. | 2014-07-31 |
20140214095 | SYSTEMS AND DEVICES FOR THE REDUCTION AND ASSOCIATION OF BONES - In accordance with the disclosed subject matter, a medical device is provided which comprises a body having a first end and a second end, a first engaging member positioned adjacent the first end of the body and adapted to operatively engage a bone, and a second engaging member positioned adjacent the first end of the body and adapted to operatively engage the bone, wherein the position of at least one engaging member is adjustable with respect to the body. | 2014-07-31 |
20140214096 | CAPS FOR IMPLANTS, IMPLANT ASSEMBLIES, AND METHODS OF USE - An implant assembly can include an implant configured to be coupled to at least one bone part. The implant can include an implant body that defines at least one unsmooth surface. The assembly can further include a cap configured to be coupled to the implant body such that the cap overlies the at least one unsmooth surface. The cap can include a shell that defines a cavity that is configured to receive at least a portion of the implant body such that the shell flexes relative to the implant body as the cavity receives the at least a portion of the implant body to thereby couple the cap to the implant. The cap defines an outer surface that is curved. | 2014-07-31 |
20140214097 | DUAL MEDICAL IMPLANT CLOSURE DRIVE SYSTEM - A two-piece closure for polyaxial bone screws includes an outer fastener and an inner set screw, the outer fastener having a drive system with pockets that cooperate with a pronged drive tool. The polyaxial screw includes a lower pressure insert engaged with the outer fastener, the insert in some embodiments being made from a cobalt chrome alloy. | 2014-07-31 |
20140214098 | MODULAR LAG SCREW - An elongated modular implant is provided which has a distal part and a proximal part both having a leading end and a trailing end, respectively. The trailing end of the distal part includes a tool engagement portion and the leading end of the proximal part includes a distal part engagement portion for an engagement with the tool engagement portion of the distal part. The implant further includes an assembly element for firmly coupling the distal part and the proximal part when the first tool engagement portion of the distal part engages the distal part engagement portion of the proximal part. The proximal part trailing end may also have a tool engagement portion identical to the trailing end of the distal part. | 2014-07-31 |
20140214099 | PEDICLE SCREW - A screw, comprising a head, and a shaft, wherein the shaft comprised a first threaded shaft portion; a second threaded shaft portion disposed contiguous to said head; and a middle shaft portion disposed between said first threaded shaft portion and said second threaded shaft, wherein said middle shaft portion is an irregular form. | 2014-07-31 |
20140214100 | ORTHOPAEDIC TOOL HANDLE AND METHOD OF MANUFACTURING SAME - An orthopaedic tool includes a handle having an exterior profile defined by a first three-dimensional shape having an exterior surface of revolution about a first axis of rotation, and a second three-dimensional shape having an exterior surface of revolution about a second axis of rotation. The second axis of rotation is offset from the first axis of rotation, whereby the first three-dimensional shape and the second three-dimensional shape intersect to define a volume of intersection. The exterior profile is defined only by the volume of intersection. A shaft extends from the handle. | 2014-07-31 |
20140214101 | CAM LOCK - An aiming device includes a body extending longitudinally from a first end to a second end and including a first body opening extending laterally therethrough along a first axis, the first body opening being sized and shaped to receive a device therein, the first end of the body including a coupling for coupling the body to an implantable device in an aiming configuration in which the first body opening is aligned with a corresponding first implant opening extending through the implantable device so that a device inserted through the first body opening in the body will pass along an axis of the first implant opening and a lock releasably coupled to the body and movable relative thereto between an unlocked and a locked configuration, the lock including an engaging portion extending into the first body opening in the locked configuration to engage an outer surface of a device received therein to lock the device in a desired position within the first body opening. | 2014-07-31 |
20140214102 | Method and System for Identification of a Center of a Vertebral Disc Space and Corresponding Central Axis of a Spinal Column - An apparatus for locating a central axis of a spinal column and method of using the same is disclosed. The apparatus and method includes one or more members capable of spanning a center line which may then be identified by at least one additional member positioned therebetween. Furthermore, the device may contain or be capable of accommodating various additional tools for marking the location of the central axis of a spinal column. | 2014-07-31 |
20140214103 | PECTUS BAR STABILIZER - An assembly for surgically treating a chest-wall deformity may include an implantable stabilizer member, an implantable pectus bar and an implantable stopping member. The implantable stabilizer member may include first and second base parts and a channel defined by the first and second base parts. The stabilizer member may include first and second retaining bars extending between the first and second base parts and traversing the channel. The first and second base parts may be adapted to be secured to tissue of the chest wall. The implantable pectus bar may be receivable within the channel of the stabilizer member. The implantable stopping member may be adapted to be engaged with the pectus bar between the first and second retaining bars after the pectus bar is inserted into the channel to restrict movement of the pectus bar relative to the tissue. | 2014-07-31 |
20140214104 | SYSTEMS AND METHODS FOR LEADLESS PACING AND SHOCK THERAPY - Techniques and systems for monitoring cardiac arrhythmias and delivering electrical stimulation therapy using a subcutaneous implantable cardioverter defibrillator (SICD) and a leadless pacing device (LPD) are described. For example, the SICD may detect a tachyarrhythmia within a first electrical signal from a heart and determine, based on the tachyarrhythmia, to deliver anti-tachyarrhythmia shock therapy to the patient to treat the detected arrhythmia. The LPD may receive communication from the SICD requesting the LPD deliver anti-tachycardia pacing to the heart and determine, based on a second electrical signal from the heart sensed by the LPD, whether to deliver anti-tachycardia pacing (ATP) to the heart. In this manner, the SICD and LPD may communicate to coordinate ATP and/or cardioversion/defibrillation therapy. In another example, the LPD may be configured to deliver post-shock pacing after detecting delivery of anti-tachyarrhythmia shock therapy. | 2014-07-31 |
20140214105 | TANDEM SERIES COUPLED IMPLANTABLE SUBCUTANEOUS CARDIOVERTER DEFIBRILLATORS AND METHOD - An implantable subcutaneous cardioverter defibrillator system for therapeutically stimulating a portion of a patient's body. First and second implantable subcutaneous cardioverter defibrillators are coupled together with a conductor. The first implantable subcutaneous cardioverter defibrillator is configured to deliver therapeutic energy in a first polarity between a first electrode and the conductor. The second implantable subcutaneous cardioverter defibrillator is configured to deliver therapeutic energy in a second polarity, opposite of said first polarity, between a second electrode and the conductor. The system is configured to synchronize delivery of the therapeutic energy by the first implantable subcutaneous cardioverter defibrillator and delivery of the therapeutic energy by the second implantable subcutaneous cardioverter defibrillator. | 2014-07-31 |
20140214106 | BUTTSTOCK - A buttstock includes a main body and a protecting member. The main body includes a shell member and an automated external defibrillator disposed in the shell member. The protecting member is movably connecting with the shell member of the main body so as to move relative to the shell member between a first position and a second position, wherein the protecting member shields the automated external defibrillator at the first position and exposes the automated external defibrillator at the second position respectively. | 2014-07-31 |
20140214107 | DYNAMIC BATTERY MANAGEMENT IN AN IMPLANTABLE DEVICE - One aspect of this disclosure relates to a system for dynamic battery management in implantable medical devices. An embodiment of the system includes two or more devices for measuring battery capacity for an implantable medical device battery. The embodiment also includes a controller connected to the measuring devices. The controller is adapted to combine the measurements from the measuring devices using a weighted average to determine battery capacity consumed. According to various embodiments, at least one of the measuring devices includes a coulometer. At least one of the measuring devices includes a capacity-by-voltage device, according to an embodiment. The system further includes a display in communication with the controller in various embodiments. The display is adapted to provide a depiction of battery longevity in units of time remaining in the life of the implantable medical device battery, according to various embodiments. Other aspects and embodiments are provided herein. | 2014-07-31 |
20140214108 | IMPLANTABLE MEDICAL DEVICE VOLTAGE DIVIDER CIRCUIT FOR MITIGATING ELECTROMAGNETIC INTERFERENCE - An RF protection circuit mitigates potentially adverse effects that may otherwise result from electromagnetic interference (e.g., due to MRI scanning of a patient having an implanted medical device). The RF protection circuit may comprise a voltage divider that is deployed across a pair of cardiac electrodes that are coupled to internal circuitry of the implantable medical device. Each leg of the voltage divider may be referenced to a ground of the internal circuit, whereby the different legs are deployed in parallel across different circuits of the internal circuitry. In this way, when an EMI-induced (e.g., MRI-induced) signal appears across the cardiac electrodes, the voltages appearing across these circuits and the currents flowing through these circuits may be reduced. The RF protection circuit may be used in an implantable medical device that employs a relatively low capacitance feedthrough to reduce EMI-induced (e.g., MRI-induced) current flow in a cardiac lead. | 2014-07-31 |
20140214109 | USING TELEMETRY DOWNLINK FOR REAL TIME CLOCK CALIBRATION - An implantable medical device includes a local clock generator for generating a system clock signal. The local clock generator is periodically calibrated to maintain accuracy of the generated system clock signal. A clocking circuit is coupled to the local clock generator to provide the calibration factor for calibrating the local clock generator. The implantable medical device receives an accurate clock signal that is transmitted from an external device and the accurate clock signal is provided to the clocking circuit. The system clock signal is also provided to the clocking circuit and a computation is performed to derive the calibration factor. | 2014-07-31 |
20140214110 | SYSTEMS AND METHODS TO MONITOR AND TREAT HEART FAILURE CONDITIONS - An implantable device monitors and treats heart failure, pulmonary edema, and hemodynamic conditions and in some cases applies therapy. In one implementation, the implantable device applies a high-frequency multi-phasic pulse waveform over multiple-vectors through tissue. The waveform has a duration less than the charging time constant of electrode-electrolyte interfaces in vivo to reduce intrusiveness while increasing sensitivity and specificity for trending parameters. The waveform can be multiplexed over multiple vectors and the results cross-correlated or subjected to probabilistic analysis or thresholding schemata to stage heart failure or pulmonary edema. In one implementation, a fractionation morphology of a sensed impedance waveform is used to trend intracardiac pressure to stage heart failure and to regulate cardiac resynchronization therapy. The waveform also provides unintrusive electrode integrity checks and 3-D impedancegrams. | 2014-07-31 |
20140214111 | Implantable Electroacupuncture Device and Method for Treating Cardiovascular Disease - An implantable electroacupuncture device (IEAD) treats heart failure, coronary artery disease, myocardial ischemia or angina through application of stimulation pulses applied at acupoints GV20 and/or EXHN3. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio of T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214113 | Implantable Electroacupuncture Device - An implantable electroacupuncture device (IEAD) treats a medical condition of a patient through application of electroacupuncture (EA) stimulation pulses applied at a target tissue location, such as an acupoint. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates EA stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214114 | IMPLANTABLE ELECTROACUPUNCTURE DEVICE AND METHOD FOR REDUCING HYPERTENSION - An implantable electroacupuncture device (IEAD) treats hypertension through application of stimulation pulses applied at at least one of acupoints PC5, PC6, ST36, or ST37. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214115 | Implantable Electroacupuncture System and Method for Reducing Hypertension - An implantable electroacupuncture device (IEAD) treats hypertension through application of stimulation pulses applied at at least one of acupoints PC5, PC6, LI4, ST36, ST37, LI11, LR3, and GB34. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214116 | Stimulation Paradigm To Improve Blood Pressure Dipping In An Implantable Electroacupuncture Device - A coin-sized implantable electroacupuncture (EA) device defines a stimulation paradigm, or stimulation regimen, that controls when EA stimulation pulses are applied to a selected acupoint, or other specified tissue location, to treat hypertension or nondipping. The stimulation regimen is applied when the patient is sleeping in order to minimize or mitigate the occurrence of nondipping or reverse dipping of the patient's blood pressure. In one embodiment, medical personnel, set a timing reference marker at the time of implant that defines how much time should elapse before a nighttime stimulation window opens that allows an EA stimulation session to be applied to the patient. In another embodiment, the patient sets the time when the nighttime stimulation window opens or when the EA stimulation session begins. Typically, an EA stimulation session is applied to the patient at a low duty cycle, e.g., only once a week during the nighttime. | 2014-07-31 |
20140214117 | Implantable Electroacupuncture Device and Method for Treating Depression, Bipolar Disorder and Anxiety - An implantable electroacupuncture device (IEAD) treats depression, bipolar disorder or Anxiety through application of stimulation pulses applied at acupoints GV20 and/or EXHN3. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214118 | Implantable Electroacupuncture System and Method for Treating Depression and Similar Mental Conditions - An implantable electroacupuncture device (IEAD) treats mental illness through application of stimulation pulses applied at a specified tissue location, including at least one of acupoints GV20 and EXHN3, or their underlying nerves. In one embodiment, the IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4 is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214119 | Implantable Electroacupuncture System and Method for Treating Parkinson's Disease and Essential Tremor - An implantable electroacupuncture device (IEAD) treats Parkinson's disease or Essential Tremor through application of stimulation pulses applied at at least one of acupoints GB34 and GV20. The IEAD includes an hermetically-sealed implantable electroacupuncture (EA) device having at least two electrodes located outside of its housing. The housing contains a primary power source, pulse generation circuitry, and a sensor that wirelessly senses externally-generated operating commands. The pulse generation circuitry generates stimulation pulses as controlled, at least in part, by the operating commands sensed through the sensor. The stimulation pulses are applied to the specified acupoint or nerve through the electrodes in accordance with a specified stimulation regimen. Such stimulation regimen requires that the stimulation session be applied at a very low duty cycle not greater than 0.05. | 2014-07-31 |
20140214120 | SYSTEMS AND METHODS FOR ELECTRICAL STIMULATION OF SPHENOPALATINE GANGLION AND OTHER BRANCHES OF CRANIAL NERVES - Devices, systems and methods are disclosed for modulating cranial nerves, such as the sphenopalatine ganglion, to treat a medical condition of a patient, such as cluster headache. A stimulation device is advanced transnasally to a target site at or adjacent to the nasopharyngeal mucosa posterior to the middle turbinate. Electrical impulses are applied through one or more electrodes in the stimulation device to the target nerve sufficient to modulate the nerve and treat the medical condition. | 2014-07-31 |
20140214121 | METHOD FOR SELECTIVELY PERFORMING LOCAL AND RADIAL PERIPHERAL STIMULATION - A control system for use with a neurostimulator comprises a user interface for receiving an input from a user and a controller. The user interface has a first control and a second control. The controller is configured for, in response to actuating the first control, operating the neurostimulation control system in a PNFS programming mode, and for, in response to actuating the second control, operating the neurostimulation control system in a PNS programming mode. A method of providing therapy to a patient comprises initially conveying pulsed electrical current at a pulse width into a peripheral tissue region of the patient to create a side effect via stimulation of one of a nerve ending and neural axon, and subsequently conveying pulsed electrical current at an adjusted pulse width into the peripheral tissue region to create a therapeutic effect via stimulation of the other one of the nerve ending and neural axon. | 2014-07-31 |
20140214122 | Method and Apparatus for Predicting and Controlling the Percepts Induced by a Visual Prosthesis - Here we present the first model that quantitatively predicts the apparent spatial position and shape of percepts elicited by retinal electrical stimulation in humans based on the known anatomy of the retina. This model successfully predicts both the shape of percepts elicited by single electrode stimulation and the shape and relative positions of percepts elicited by multiple electrode stimulation. Model fits to behavioral data show that sensitivity to electrical stimulation is not confined to the axon initial segment, but does fall off rapidly with the distance between stimulation and the initial segment. Using the model, it is possible to compensate, preferably with a look up table, to match percepts to a desired image. | 2014-07-31 |
20140214123 | Bilateral Communication in a Two-Channel System - A hearing prosthesis system has a hearing prosthesis device for each ear. In the case of a cochlear implant, the prosthesis may have both an external portion and an internal portion. The external portion provides a wireless communication to the internal portion. Additionally, each prosthesis is configured to communicate with the other prosthesis. Thus, a second wireless signal provides a bilateral communication link between the two prostheses. Advantageously, in order to mitigate potential wireless interference due to each prosthesis communicating with both a corresponding internal component and the other external component, the disclosed systems and methods operate in a specific communication mode. Under this mode, for each time period, one external component is in a transmit mode, while the other external component is in a receive mode. As the time period advances, the external components simultaneously switch modes. | 2014-07-31 |
20140214124 | Implantable Electroacupuncture System and Method for Treating Cardiovascular Disease - An implantable electroacupuncture device (IEAD) treats cardiovascular disease through application of stimulation pulses applied at at least one of acupoints EX-HN1, BL14, HT7, HT5, PC6, ST36, LI11, LU7 and LU2. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4 is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214125 | Implantable Electroacupuncture System and Method for Treating Dyslipidemia and Obesity - An Implantable ElectroAcupuncture System (IEAS) treats dyslipidemia or obesity through application of stimulation pulses applied at at least one of acupoints ST36, SP4, ST37, ST40, SP6, SP9, K16, or LR8, or underlying nerves saphenous or peroneal. The IEAS includes an hermetically-sealed implantable electroacupuncture (EA) device having at least two electrodes located outside of its housing. The housing contains a primary power source, pulse generation circuitry, and a sensor that wirelessly senses externally-generated operating commands. The pulse generation circuitry generates stimulation pulses as controlled, at least in part, by the operating commands sensed through the sensor. The stimulation pulses are applied to the specified acupoint or nerve through the electrodes in accordance with a specified stimulation regimen. Such stimulation regimen requires that the stimulation session be applied at a very low duty cycle not greater than 0.05. | 2014-07-31 |
20140214126 | Implantable Electroacupuncture Device and Method for Treating Obesity - An implantable electroacupuncture device (IEAD) treats obese conditions of a patient through application of stimulation pulses applied at acupoints SP4, LR8 or ST40, or their underlying nerves saphenous and peroneal. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214127 | Implantable Electroacupuncture Device and Method for Treating Dyslipidemia - An Implantable ElectroAcupuncture Device (IEAD) treats dyslipidemia conditions of a patient through application of stimulation pulses applied at acupoint ST40, or its underlying nerves saphenous and peroneal. The IEAD comprises an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214128 | Circuits and Methods for Using a High Impedance, Thin, Coin-Cell Type Battery in an Implantable Electroacupuncture Device - An implantable electroacupuncture device (IEAD) treats a disease or medical condition of a patient through application of stimulation pulses applied at a specified acupoint or other target tissue location. In a preferred implementation, the IEAD is an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214129 | ENERGY EFFICIENT NEUROMODULATION - A therapy system for applying an electrical signal to a target nerve includes an electrode, an implantable component and an external component. The electrode has an impedance of at least about 2000 ohms. The electrical signal is applied using constant current or constant voltage. | 2014-07-31 |
20140214130 | RF RESISTANT FEEDTHROUGH ASSEMBLY AND ELECTRICAL STIMULATION SYSTEMS CONTAINING THE ASSEMBLY - A control module for an electrical stimulation system includes a casing having an electrically-conductive portion; an electronic subassembly disposed in the casing; and a header portion coupled to the casing and including a connector for a lead or lead extension. The control module also includes a feedthrough assembly coupling the casing to the header portion. The feedthrough assembly includes a non-conductive ceramic block; conductive feedthrough pins passing through the ceramic block and electrically coupling the connector to the electronic subassembly disposed in the casing; a metal flange disposed around, and attached to, the ceramic block, and a non-conductive spacer attached to the metal flange and to the casing to raise the ceramic block above, and away from, the casing. Other control modules include a ceramic block that has a rim portion that raises the plate portion, through which the feedthrough pins pass, of the block away from the casing. | 2014-07-31 |
20140214131 | APPARATUS AND METHODS FOR DETECTING MIGRATION OF NEUROSTIMULATION LEADS - Apparatus and methods for detecting lead migration through the use of measured artifactual data about the tissue in the vicinity of the lead. | 2014-07-31 |
20140214132 | IMPLANTABLE MEDICAL DEVICE CHARGING - A particular method of providing power to an implantable medical device includes providing a first signal to a primary coil that is inductively coupled to a secondary coil of an implantable medical device. The method also include determining a first alignment difference between a voltage corresponding to the first signal and at least one of a current corresponding to the first signal and a component voltage at a component of a primary coil circuit. The method further includes determining a frequency sweep range based on the first alignment difference. The method also includes performing a frequency sweep over the frequency sweep range. | 2014-07-31 |
20140214133 | Radial Feed Through Packaging For An Implantable Electroacupuncture Device - An implantable electroacupuncture device (IEAD) treats a disease or medical condition of a patient through application of stimulation pulses applied at a specified acupoint or other target tissue location. In a preferred implementation, the IEAD is an implantable, coin-sized, self-contained, leadless electroacupuncture device having at least two electrodes attached to an outside surface of its housing. The device generates stimulation pulses in accordance with a specified stimulation regimen. Power management circuitry within the device allows a primary battery, having a high internal impedance, to be used to power the device. The stimulation regimen generates stimulation pulses during a stimulation session of duration T3 minutes applied every T4 minutes. The duty cycle, or ratio T3/T4, is very low, no greater than 0.05. The low duty cycle and careful power management allow the IEAD to perform its intended function for several years. | 2014-07-31 |
20140214134 | Closed Loop Chronic Electroacupuncture System Using Changes in Body Temperature or Impedance - A closed loop electroacupuncture (EA) system monitors any change in sympathetic drive within the body of a patient undergoing EA stimulation. The sensed change in sympathetic drive is then used to adjust at least one parameter of the EA stimulation regimen in an appropriate manner that assists regulation of the patient's autonomic nervous system (ANS). One manner of determining an increase in sympathetic drive is to monitor the body temperature at the skin. A decrease in skin temperature is indicative of increased sympathetic drive and/or exercise stress due to vasoconstriction in the subcutaneous vascular bed. An adjunct to monitoring skin temperature is to monitor subcutaneous tissue impedance. Subcutaneous tissue impedance increases during vasoconstriction. Thus, a sensed change in tissue impedance may be used by itself, or as a compliment to sensed changes in temperature, to provide feedback within the closed loop EA system to adjust the stimulation regimen. | 2014-07-31 |
20140214135 | DISSOLVABLE ELECTRODE DEVICE - An electrode assembly is provided that is configured to be coupled to nervous tissue of a subject, the electrode assembly including one or more conductive elements. At least a portion of the electrode assembly, including the conductive elements, is configured to be dissolvable after the electrode assembly has been coupled to the tissue. The electrode assembly is configured to come loose from the tissue upon dissolving of the dissolvable at least a portion thereof. Other embodiments are also described. | 2014-07-31 |
20140214136 | Pulse Width Modulation Control for Battery-Powered Laser Device - A battery-powered laser-based dermatological treatment device may include a laser unit comprising at least one laser diode, a battery unit, at least one sensor configured to generate sensor signals, and a laser drive control system including a laser drive circuit comprising the laser unit, the battery unit, a first switch (e.g., a first FET), and a second switch (e.g., a second FET), wherein the laser unit is arranged in series between the first switch and the second switch, and control electronics configured to control the first switch based at least on sensor signals from the at least one sensor, and control the second switch using pulse width modulation (PWM), thereby delivering current from the battery unit to the laser unit with a PWM current waveform. The laser drive circuit may also include a snubber circuit configured to prevent voltage spikes upon the second switch being turned off. | 2014-07-31 |
20140214137 | acupuncture and moxibustion apparatus with multi-frequency microwave - The present invention discloses an acupuncture and moxibustion apparatus with multi-frequency microwave comprising a microwave oscillator A, a power amplifier A, circulator A, a power divider A, a microwave radiator A, a microwave oscillator B, a power amplifier B, a circulator B, a power divider B, a microwave radiator B, a controller, a display screen, and a power supply unit. Two medical frequencies in the international microwave band L are used to avoid the interferences between communication and TV. And the solid state modular microwave source is used, which provides a good thermal penetration, heating homogeneity, and safety performance, as well as high efficiency and long service life. Dual effect of acupuncture using metal needle and heating of acupuncture points by moxibustion is provided. The apparatus can be used to treat multiple human diseases. | 2014-07-31 |
20140214138 | HYBRID MEDICAL COOLING PAD WITH INCREASED WATER FLOW AREA - A medical pad having a dual layer portion including a fluid circulation and containment layers and a single layer portion including the fluid circulation layer. The fluid circulation layer is for containing a first thermal-exchange fluid circulatable therethrough, with the medical pad being operable for thermal exchange between the first thermal-exchange fluid and a patient through a first side of the fluid circulation layer. A fluid containment layer of the medical pad is interconnected to a portion of second side of the fluid circulation layer, opposite to the first side of the fluid circulation layer. The fluid containment layer encloses a second thermal-exchange fluid that may have a freezing point of 0° C. or less. Portions of the fluid circulation layer that extend beyond the fluid containment layer define flaps that provide additional area for fluid circulation. | 2014-07-31 |
20140214139 | TISSUE COOLING CLAMPS AND RELATED METHODS - Methods and devices are disclosed herein that generally involve cooling tissue (e.g., localized cooling of tissue), and in particular applying therapeutic hypothermia to the spinal canal, tissue disposed within the spinal canal, and/or nerve roots extending from the spinal canal. In some embodiments, tissue can be cooled by clamping a cooling instrument to a bone or implant that is proximate to the tissue. The cooling instrument can define a chamber through which a chilled fluid, expandable gas, or other coolant means can be circulated, delivered, or activated to cool adjacent tissue. The degree of cooling can be regulated using a controller, which can be configured to increase or decrease the cooling effect based on any of a variety of measured or predicted physiological or thermodynamic properties. Methods are disclosed for utilizing cooling instruments and for carrying out various treatment regimens that involve cooling tissue using such instruments. | 2014-07-31 |
20140214140 | METHOD AND APPARATUS FOR CONTROLLING A PATIENT'S BODY TEMPERATURE BY IN SITU BLOOD TEMPERATURE MODIFICATION - The present invention provides a method and apparatus for controlling the internal body temperature of a patient. According to the present invention, a catheter is inserted through an incision into a large blood vessel of a patient. By selectively heating or cooling a portion of the catheter lying within the blood vessel, heat may be transferred to or from blood flowing within the vessel and the patient's body temperature may thereby be increased or decreased as desired. The invention will find use in treating undesirable conditions of hypothermia and hyperthermia, or for inducing a condition of artificial hypothermia when desired. The method and system further provide for the cooling of initially hypothermic patients whose blood or body temperature has been warmed above the desired target level and the warming of initially hyperthermic patients whose blood or body temperature has been cooled below the desired target temperature. | 2014-07-31 |
20140214141 | UNDERBODY CONVECTIVE BLANKET - A full body convective blanket has a head portion, a body portion and a foot portion. The head and foot portions each taper in a decreasing manner from a corresponding opposite side of the body portion to the head and foot ends, respectively, so that the blanket has a rectangular shaped body portion and head and foot portions that are shaped in the form of isosceles trapezoids. Two elongate openings are provided longitudinally along the body portion sandwiching a non-inflatable area. An opening is provided at the head portion of the blanket. | 2014-07-31 |
20140214142 | TREATMENT SYSTEM - A treatment system includes a holding section that has a heat generation section for applying thermal energy and holds a living tissue, a signal output section that supplies a drive signal to the heat generation section, a signal detection section that detects the drive signal, a signal extraction section that extracts an extracted signal of a predetermined frequency band from the drive signal detected by the signal detection section, a fault detection section that detects when a precursory phenomenon of a fault of the heat generation section the extracted signal reaches or exceeds a predetermined threshold, and a control section that performs control, when the fault detection section detects the precursory phenomenon, so as to reduce power of the drive signal supplied from the signal output section to the heat generation section. | 2014-07-31 |
20140214143 | ELECTROSTIMULATION IN TREATING CEREBROVASCULAR CONDITIONS - An electrostimulation device including an electrode shaft that includes a plurality of electrodes, a delivery device that includes a cannula, through which the electrode shaft is insertable, a fixation member fixable on the cannula, and a locking mechanism for selectively permitting and preventing relative movement between the electrode shaft and the delivery device. | 2014-07-31 |
20140214144 | Electrode Configuration for an Implantable Electroacupuncture Device - An implantable electroacupuncture device (IEAD) treats a disease or medical condition of a patient through application of stimulation pulses applied at a specified acupoint or other target tissue location at a very low duty cycle. In a preferred implementation, the IEAD is an implantable, coin-sized, self-contained, leadless device having at least two electrodes attached to an outside surface of its housing, with at least one electrode on the top or bottom surface of the housing functioning as a cathode, and at least one electrode on the perimeter edge of the housing functioning as an anode. The electrodes may be segmented to include an array of smaller cathodic or anodic electrodes, each of which may be selectively turned ON or OFF so as to provide a convenient mechanism for adjusting the density of the stimulus current flowing through the cathodic electrode surface area. | 2014-07-31 |
20140214145 | Impact Protection for Implantable Electric Lead - A novel implantable electric lead arrangement is described for medical implant systems such as middle ear implants (MEI), cochlear implants (CI) and vestibular implants (VI). An electric lead contains parallel lead wires wound in an elongated helix about a central longitudinal axis. A lead core is fixed and enclosed within the wire helix for providing impact strain relief to the lead wires by resisting radial and/or axial deformation from external impact force. | 2014-07-31 |
20140214146 | METHOD FOR TREATING A TARGET SITE IN A VASCULAR BODY CHANNEL - A method of treating a target site within a vascular channel of the body uses a catheter assembly having proximal and distal occluders which are positioned in occluding states at positions proximal and distal of a target site to define an occluded region therebetween. An agent is injected into the region. An intervention is performed at the target site while the vessel is occluded and the agent is in the region. The catheter assembly is removed from the channel. Intervention may include expanding a balloon within a temporary stent structure against the channel, collapsing balloon and then removing the collapsed balloon and stent structure from the channel. A balloon stent assembly comprises a catheter assembly, a temporary stent surrounding a balloon, the temporary stent placeable in a contracted state by the catheter assembly and in an expanded state by inflation of the balloon. | 2014-07-31 |
20140214147 | Stent System, Deployment Apparatus and Method for Bifurcated Lesion - A deployment apparatus and method for deploying one or more stents to a bifurcated vessel is provided. The invention is particularly suited for T-type bifurcated vessels where a side branch extends from a main branch. The deployment apparatus has a primary inflatable portion for engagement within the main branch and a secondary inflatable portion for engagement within the side branch. A main stent is arranged on the primary inflatable portion and radially expanded within the main branch while the secondary inflatable portion maintains registration with the side branch. A side branch stent is then arranged on the secondary inflatable portion and expanded within the side branch while the primary inflatable portion maintains registration with the expanded main stent. A bifurcated stent system suitable for bifurcated lesions is also provided comprising a side branch stent with a shaped end designed to engage a similarly shaped side opening in a main stent. | 2014-07-31 |
20140214148 | PROSTHESIS DELIVERY SYSTEM - Disclosed herein are implantable, radially expandable medical prostheses, including but not limited to stents, and delivery and loading systems applicable to the same, including disposable, detachable distal chambers, and methods for using the same. | 2014-07-31 |
20140214149 | METHOD AND APPARATUS FOR MEASURING FLOW THROUGH A LUMEN - A prosthesis for monitoring a characteristic of flow includes a first tubular prosthesis having a lumen and a sensor for detecting the characteristic of flow through the lumen. The sensor may be covered with another tubular prosthesis or by a layer of material in order to insulate the sensor from the fluid flow. A pocket may be formed between the tubular prosthesis and the adjacent layer of material or prosthesis and the sensor may be disposed in the pocket. | 2014-07-31 |
20140214150 | ANTI-MIGRATION STENT WITH QUILL FILAMENTS - A stent that includes a plurality of quill filaments. Each quill filament includes filament material, a surface, and a plurality of quills. Each quill has a tip, a body, and a base where the body extends from the base to the tip. The quill filaments can be interwoven to form the stent or the quill filaments can be engaged to the framework of a stent. | 2014-07-31 |
20140214151 | DELIVERY DEVICE DISTAL SHEATH CONNECTOR - A connector for coupling a distal sheath to an inner shaft of a medical delivery device includes a wedge defining a lumen for accepting the inner shaft of the medical delivery device and a cylindrical ring sized to mate with the wedge. The wedge may be welded or otherwise fixed to the inner shaft. The wedge and the ring are configured to be pressed together and lock a portion of the distal sheath therebetween. | 2014-07-31 |
20140214152 | METHOD AND DEVICE FOR HEART VALVE REPAIR - A repair device for repairing a heart valve leaflet in a patient includes a hollow body with a capture tool and a tissue puncture element at the distal end thereof. The capture tool may be used to capture and stabilize the heart valve leaflet tissue. The tissue puncture element may puncture the leaflet tissue and deploy at least one anchor having a length of suture attached thereto. By tensioning the suture, the leaflet tissue may become plicated. The tensioned suture may then be cinched to maintain the plication. | 2014-07-31 |
20140214153 | Methods of implanting an endoprosthesis - A catheter is disclosed for the transvascular implantation of prosthetic heart valves, e.g., including self-expanding anchorage supports, to reduce the risk to the patient during the implantation. Accordingly, a prosthetic heart valve comprising anchorage supports is temporarily housed in a folded form in a cartridge-type unit during the implantation. The cartridge-type unit can be fixed on the proximal end of a guide system, which comprises a flexible region that can be guided through the aorta. Actuating elements run through the interior of the hollow guide system, permitting sections of the cartridge-type unit to be displaced radially about their longitudinal axis and/or laterally in a proximal direction, thus allowing individual sections of the anchorage support and the associated prosthetic heart valve to be sequentially released. | 2014-07-31 |
20140214154 | Methods for delivering a self-expanding valve - Methods for delivering a prosthetic heart valve include advancing a delivery catheter containing the prosthetic heart valve to a deployment location at a native heart valve, advancing an inner core movably coupled to a restraining sheath of the delivery catheter to expose a first end of the prosthetic heart valve, and advancing the inner core and the restraining sheath to expose a second end of the prosthetic heart valve. The delivery catheter can include a distal flange located at a distal end of an outer core of the catheter body, configured to restrict distal longitudinal displacement of the prosthetic heart valve, and a retaining structure located proximally from the distal flange along the outer core of the catheter body, configured to restrict proximal longitudinal displacement of the prosthetic heart valve. | 2014-07-31 |
20140214155 | Methods For Deployment Of Medical Devices - Methods for delivering a medical device loaded onto a catheter include positioning a first tube relative to a second concentric tube such that sheathing material having a first end affixed to the first tube and a second end affixed to the second tube forms an inner layer and an outer layer having at least one inversion point, such that no portion of the first tube is between any portion of the inner and outer layers of the sheathing material. Upon positioning the catheter at a desired target site, the first tube can be moved relative to the second tube so that the inversion point moves to expose the medical device, thereby permitting expansion of the medical device at the target site. | 2014-07-31 |
20140214156 | APPARATUS AND METHOD FOR REPLACING A DISEASED CARDIAC VALVE - An apparatus for replacing a diseased cardiac valve is movable from a radially collapsed configuration to a radially expanded configuration. The apparatus comprises an expandable support member and a prosthetic valve secured therein. The main body portion extends between first and second end portions and includes an outer circumferential surface, a circumferential axis extending about the circumferential surface, and a plurality of wing members spaced apart from one another by an expandable region. Each of the wing members includes first and second end portions and a flexible middle portion extending between the end portions. The second end portion is integrally formed with the uyimain body portion. The first end portion is adjacent the circumferential axis and substantially flush with the outer circumferential surface in the radially collapsed configuration. The first end portion extends substantially radial to the outer circumferential surface in the radially expanded configuration. | 2014-07-31 |
20140214157 | TRANSCATHETER VALVE PROSTHESIS - A transcatheter atrio-ventricular valve prosthesis for functional replacement of an atrio-ventricular heart valve in a connection channel, the prosthesis comprising a radially expandable tubular body extending along an axis, and a valve arranged within and attached to the tubular body. The tubular body is provided with an outer circumferential groove which is open to the radial outside of the tubular body, whereby the tubular body is separated by the outer circumferential groove into first and second body sections. The tubular body is provided with a first plurality of projections which extend from the first or second body section in an axial direction of the tubular body and each of which has a free end arranged to overlap the outer circumferential groove. An elongate outer member may be disposed at the exterior of the connection channel wall structure at a level of the circumferential groove. | 2014-07-31 |
20140214158 | SURGICAL HEART VALVE FLEXIBLE STENT FRAME STIFFENER - A prosthetic heart valve includes an annular frame having annularly spaced commissure portions and an annulus portion disposed near an inflow edge, a fabric covering at least a portion of the frame and a valve assembly connected to the frame at the commissure portions, the valve assembly including a plurality of leaflets. A stiffening member is disposed about the frame to limit ovalization of the frame when a radial force is applied to the frame. | 2014-07-31 |
20140214159 | PROSTHETIC VALVES AND RELATED INVENTIONS - This invention relates to the design and function of a compressible valve replacement prosthesis, collared or uncollared, 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. | 2014-07-31 |
20140214160 | HEART VALVE PROSTHESIS WITH COLLAPSIBLE VALVE AND METHOD OF DELIVERY THEREOF - A valve prosthesis is adapted to operate in conjunction with native heart valve leaflets. The prosthesis includes an annulus and a skirt extending from the annulus. The skirt may be configured to be positioned through a native heart valve annulus, and the skirt may be movable between an open configuration permitting blood flow through the skirt and a closed configuration blocking blood flow through the skirt in cooperation with opening and closing of the native heart valve leaflets. | 2014-07-31 |
20140214161 | OCULAR IMPLANTS WITH ASYMMETRIC FLEXIBILITY - An ocular implant having an inlet portion and a Schlemm's canal portion distal to the inlet portion, the inlet portion being disposed at a proximal end of the implant and sized and configured to be placed within an anterior chamber of a human eye, the Schlemm's canal portion being arranged and configured to be disposed within Schlemm's canal of the eye when the inlet portion is disposed in the anterior chamber. | 2014-07-31 |
20140214162 | ANIMATRONIC EYE WITH AN ELECTROMAGNETIC DRIVE AND FLUID SUSPENSION AND WITH VIDEO CAPABILITY - An animatronic eye with fluid suspension, electromagnetic drive, and video capability. The eye assembly includes a spherical, hollow outer shell that contains a suspension liquid. An inner sphere is positioned in the outer shell in the suspension liquid to be centrally floated at a distance away from the shell wall. The inner sphere includes painted portions providing a sclera and iris and includes an unpainted rear portion and front portion or pupil. The shell, liquid, and inner sphere are have matching indices of refraction such that interfaces between the components are not readily observed. A camera is provided adjacent a rear portion of the outer shell to receive light passing through the shell, liquid, and inner sphere. A drive assembly is provided including permanent magnets on the inner sphere that are driven by electromagnetic coils on the outer shell to provide frictionless yaw and pitch movements simulating eye movements. | 2014-07-31 |
20140214163 | TISSUE GRAFT FIXATION - A tissue graft fixation device including a body having an upper and lower surface, a first end portion, a second end portion, and an intermediate portion extending between the first and second end portions, the intermediate portion comprising at least two tabs extending transverse to the intermediate portion, the intermediate portion defining at least one hole located between the at least two tabs, and each of the at least two tabs comprising a keel extending transverse to the intermediate portion and including a cutting edge. | 2014-07-31 |
20140214164 | PERCUTANEOUS ARTHRODESIS METHOD AND SYSTEM - A method and system for percutaneous fusion to correct disc compression is presented. The method has several steps, for instance, inserting a percutaneous lumbar interbody implant; positioning guide wires for each facet screw to be implanted; performing facet arthrodesis in preparation for the facet screws; fixating the plurality of facet screws; and optionally performing foramen nerve root or central decompression. The system includes an implant, an elongate cannulated insertion tool, and an elongate lockshaft positioned within the insertion tool. | 2014-07-31 |
20140214165 | PERCUTANEOUS ARTHRODESIS METHOD AND SYSTEM - A method and system for percutaneous fusion to correct disc compression is presented. The method has several steps, for instance, inserting a percutaneous lumbar interbody implant; positioning guide wires for each facet screw to be implanted; performing facet arthrodesis in preparation for the facet screws; fixating the plurality of facet screws; and optionally performing foramen nerve root or central decompression. The system includes an implant, an elongate cannulated insertion tool, and an elongate lockshaft positioned within the insertion tool. | 2014-07-31 |
20140214166 | SPINAL IMPLANTS, SPINAL IMPLANT KITS, AND SURGICAL METHODS - A spinal implant includes a body, plate, and bone screws. The body includes a first wall having second and third walls joined thereto to define legs. In an embodiment, the body and plate are of unitary construction. In alternative embodiments, the body is formed from a first material and is configured for positioning between vertebral bodies. In other embodiments, the body is separate from the plate. The plate has a main portion and a flange. The main portion has a first screw hole oriented towards the first vertebral body at an oblique angle relative to the horizontal axis of the body. The flange has a second screw hole oriented towards the second vertebral body and substantially parallel to the horizontal axis. The flange is coupled to the main portion and extends past the main portion. Each bone screw is insertable through a screw hole of the plate for attachment to bone. A kit including a body, bone screws, and a plurality of different plates is also provided. | 2014-07-31 |
20140214167 | SPINAL IMPLANTS, SPINAL IMPLANT KITS, AND SURGICAL METHODS - A spinal implant includes a body, plate, and bone screws. The body includes a first wall having second and third walls joined thereto to define legs. In an embodiment, the body and plate are of unitary construction. In alternative embodiments, the body is formed from a first material and is configured for positioning between vertebral bodies. In other embodiments, the body is separate from the plate. The plate has a main portion and a flange. The main portion has a first screw hole oriented towards the first vertebral body at an oblique angle relative to the horizontal axis of the body. The flange has a second screw hole oriented towards the second vertebral body and substantially parallel to the horizontal axis. The flange is coupled to the main portion and extends past the main portion. Each bone screw is insertable through a screw hole of the plate for attachment to bone. A kit including a body, bone screws, and a plurality of different plates is also provided. | 2014-07-31 |
20140214168 | INTERVETERBRAL DISC PROSTHESIS INSERTION ASSEMBLIES - In various embodiments, an intervertebral disc prosthesis is provided. The prosthesis may be provided with an insertion adapter, such as a head, holder, or other carrier of the prosthesis. The insertion adapter may be configured to retain the prosthesis and to engage an insertion tool body. In various embodiments, the prosthesis and the insertion holder are provided in a sterile pack, with the prosthesis components and the insertion holder sterilized and packaged in one or more types or layers of sterile packaging. In various other embodiments, the prosthesis and an insertion tool are provided in a sterile pack, with the prosthesis components and the insertion tool sterilized and packaged in one or more types or layers of sterile packaging. | 2014-07-31 |
20140214169 | Method for Performing Implant Surgery - The joint implant manufacturer obtains and compiles surgeon-specific surgical and supply preference information in relation to a supplied joint implant prior to surgery. The manufacturer designates and trains at least one surgical team member using the surgeon-specific preference information and then supplies the service of the surgical team member(s) together with the supplied joint implant and supplies. The surgical team member(s) perform surgical procedures on the patient to assist the surgeon in removing a defective joint and replacing it with the supplied implant in accordance with the surgeon's surgical preferences. | 2014-07-31 |
20140214170 | GLENOID COMPONENT WITH OFFSET CENTER AND ASSOCIATED METHODS - A glenoid component having an offset center of articulation and associated systems and methods. | 2014-07-31 |
20140214171 | SELF-CENTERING, ANTI-SEIZING ACETABULAR LINER - A liner adapted for insertion into an acetabular shell for use in hip arthroplasty. The liner includes a concave inner surface adapted to engage a femoral head. The liner also includes an outer surface adapted to engage the acetabular shell and a rim that extends between the inner surface and the outer surface. The outer surface includes a locking section extending from the rim, a composite-curved section extending from the locking section at a first transition point, and a dome section extending from the composite-curved section, wherein at the first transition point, the composite-curved section is tangential to the locking section. | 2014-07-31 |
20140214172 | REVISION HIP PROSTHESIS HAVING AN IMPLANTABLE DISTAL STEM COMPONENT - A modular femoral prosthesis for use during performance of a hip revision procedure includes a proximal body component, a distal stem component, and a locking bolt. Surgical instruments and methods for use in implanting such a modular femoral prosthesis are disclosed. | 2014-07-31 |
20140214173 | DYNAMIC BIOACTIVE NANOFIBER SCAFFOLDING - A resorbable bone graft scaffold material, including a plurality of overlapping and interlocking fibers defining a scaffold structure, plurality of pores distributed throughout the scaffold, and a plurality of glass microspheres distributed throughout the pores. The fibers are characterized by fiber diameters ranging from about 5 nanometers to about 100 micrometers, and the fibers are a bioactive, resorbable material. The fibers generally contribute about 20 to about 40 weight percent of the scaffold material, with the microspheres contributing the balance. | 2014-07-31 |
20140214174 | PROCESS FOR PREPARING CERAMIC IMPLANTS FOR MEDICAL PURPOSES - A process for manufacturing a ceramic implant with a surface which forms a permanent bonding to bone cell tissues, the surface providing improved osseointegration, the process comprising the step of:—a pretreatment of the ceramic material with the surface wherein said surface of the ceramic material is exposed to a conditioning plasma, which is produced by means of direct current (DC) or alternating current (AC), such as high or radio frequency (HF, RF), or microwaves (MW) at a low pressure, followed by a second step;—a treatment with a reactive plasma in which an organic compound is added to the plasma for the at least partial application of an organic phase to said surface wherein the organic compound is selected from the group consisting of aliphatic amines, cyclic amines, unsaturated and aromatic amines as well as combinations thereof. | 2014-07-31 |
20140214175 | URETERAL STENT WITH DRUG-RELEASING STRUCTURE - According to one aspect of the present disclosure, ureteral stents are provided that comprise an elongated stent body, at least one deployable retention structure, and at least one sleeve and/or sheet of drug-releasing material. In various embodiments, at least one sleeve and/or sheet of drug-releasing material is deployed concurrently with the deployment of at least one deployable retention structure. The ureteral stents of the present disclosure are adapted to release the urologically beneficial drug into a subject. | 2014-07-31 |
20140214176 | PLACENTAL TISSUE GRAFTS AND IMPROVED METHODS OF PREPARING AND USING THE SAME - Described herein are tissue grafts derived from the placenta. The grafts are composed of at least one layer of amnion tissue where the epithelium layer has been substantially removed in order to expose the basement layer to host cells. By removing the epithelium layer, cells from the host can more readily interact with the cell-adhesion bio-active factors located onto top and within of the basement membrane. Also described herein are methods for making and using the tissue grafts. The laminin structure of amnion tissue is nearly identical to that of native human tissue such as, for example, oral mucosa tissue. This includes high level of laminin-5, a cell adhesion bio-active factor show to bind gingival epithelia-cells, found throughout upper portions of the basement membrane. | 2014-07-31 |
20140214177 | Transdermal Intraosseous Device - A transdermal intraosseous device for coupling a bone stump to an external prosthetic device includes a bone fixator, an external connector and a plurality of modular interface components. The bone fixator includes a proximal portion configured for anchoring into the bone stump of the patient and a distal portion including a base collar configured for subcutaneous implantation. The external connector has a distal portion for coupling to the external prosthetic device and a proximal portion for coupling to the distal portion of the bone fixator. Each interface component can be removably coupled to the base collar and has different size and shape to provide a surgeon-selected transition between the prosthetic device and the patient's skin. | 2014-07-31 |
20140214178 | CONTROL DEVICE FOR AN AUTOMATION SYSTEM - This control device is provided for an automation system comprising members to be controlled ( | 2014-07-31 |
20140214179 | METHOD OF OPERATING AN AUTOMATION SYSTEM - A method of operating an automation system cyclically communicating with a central unit in accordance with a send clock and a predetermined reduction ratio using a first cycle time, wherein the central unit uses a send clock SCC for its communication, and communicates with the automation device taking into account the send clock and a reduction ratio of the automation device, and wherein the send clock for the automation device is divided by the send clock of the central unit, the largest power-of-2 value smaller than the division result is selected and multiplied with the reduction ratio of the automation device resulting in a reduction ratio of the central unit for communicating with the automation device, and the reduction ratio of the automation device is used to step down the send clock of the central unit for cyclically communicating with the automation device using a second cycle time. | 2014-07-31 |
20140214180 | COOPERATIVE OPERATING DEVICE AND METHOD - A cooperative operating device includes primary controlling units that are provided for individual primary control systems, and calculate operating variables and outputting them to the actuators of the corresponding primary control systems, a selector that combines operating variables by performing a weighting calculation on the operating variables calculated by the primary controlling units, and an operating variable adjustment controlling unit that is provided to correspond to a single secondary control system for controlling an equilibrium point that is a desirable operating variable output with the primary control in a steady-state, inputs a specific operating variable setting value that indicates the equilibrium point, and inputs, as a controlled variable input, the operating variable after combination, outputted from the selector, to calculate an adjustment operating variable and output it to the actuator of the secondary control system. | 2014-07-31 |
20140214181 | CONTROL SYSTEM FOR SOFTWARE TERMINATION PROTECTION - The present disclosure is directed to a control system for a machine. The control system has an electronic module that includes a memory storing a control system software. The control system also includes at least one programmable controller in communication with the memory, where the at least one programmable controller is configured to protect machine components from damage by running the control system software, detecting a control system software fault, intercepting a process fault termination command, setting at least one output signal in response to the control system software fault, terminating at least part of the control system software that contains the control system software fault, and resetting at least part of the control system. | 2014-07-31 |
20140214182 | METHOD OF DETERMINING OPTIMAL TORQUE OF A FOUNDATION FASTENER - A method of determining and verifying an acceptable torque value for a foundation fastener used to secure a pair of adjacently located rotating machines having their shafts coupled together. An alignment engineer enters characteristics respective to a proposed foundation fastener into a software directed processing device. The processor analyzes the fastener characteristics when applied to the specific application of the adjacently located rotating machines to determine a target torque value. The processing device utilizes the calculated torque to determine an anticipated elongation of the fastener. The anticipated elongation is compared to an acceptable elongation range to determine if the proposed target torque value is acceptable. Once the software determines the proposed fastener and target torque value are acceptable for the application, the software informs the alignment engineer accordingly. | 2014-07-31 |
20140214183 | INDUSTRIAL PLANT PRODUCTION AND/OR CONTROL UTILIZATION OPTIMIZATION - A method includes obtaining production and control utilization information for an industrial plant, wherein the information is in an electronic format and collected over time, grouping the information, based on a type of the information, into a plurality of groups, wherein the information in each group is for a same type of information, trending the information in each group over time, aggregating the trended information, evaluating the aggregated information based on predetermined evaluation criteria, and generating an electronic signal indicating the information that satisfied the predetermined evaluation criteria and the information that did not satisfy the predetermined evaluation criteria. | 2014-07-31 |
20140214184 | Position Control for a Positioning System Comprising Larger Scale and Smaller Scale Positioning Mechanisms - A method and apparatus for controlling a positioning mechanism comprising a smaller scale positioning mechanism for moving a tool within a smaller scale work space and a larger scale positioning mechanism for changing a position of the smaller scale work space within the larger scale work space. A commanded position for the tool is received by a processor unit. An error component is determined using a difference between the commanded position and a current position of the tool in the larger scale work space. A restoring component configured to move the tool toward a selected position in the smaller scale work space is determined. Control signals for controlling the smaller scale positioning mechanism and the larger scale positioning mechanism together to move the tool from the current position to the commanded position are generated using the error component and the restoring component. | 2014-07-31 |
20140214185 | Somatosensory Household Electricity Control Equipment and System Thereof - A somatosensory household electricity control equipment and a system thereof is used in an indoor space in which a household electricity equipment is fixed. The household electricity equipment contains: a host device fixed in the indoor space; at least one action identifying device for receiving image data of the posture motion connected with the host device; a signal receiving module fixed in household electricity products and receiving a signal transmitted from the host device; and an external configuration interface used to connect with the host device so as to edit and correct data. | 2014-07-31 |
20140214186 | METHODS AND APPARATUS TO INTERFACE WITH A DIGITAL CONTROL LOOP - Example methods and apparatus to interface with a control a loop are disclosed. An example apparatus includes a loop controller to control a control loop, a sensor to provide a measurement value to the loop controller, a device controller to adjust a control device based on an output from the loop controller, and a loop interface to receive a set point value and send the set point value to the loop controller, wherein the loop interface is different from a host device communicatively coupled to the loop controller. | 2014-07-31 |
20140214187 | RC/Autonomous Machine Mode Indication - A method and system for displaying machine mode information to a remote operator of a plurality of machines includes collecting video data from each of the machines, collecting machine sensor information from each of the machines, collecting machine alert information with respect to each of the machines, and collecting machine operating mode data with respect to each of the machines. A machine display is then provided at a remote control center including one or more screen regions corresponding to the video of one or more machines. The machine display further includes a machine mode and alert indicator including machine areas associated with each of the machines, wherein each machine area including a graphical mode indicator denoting an operating mode of the associated machine. | 2014-07-31 |