06th week of 2012 patent applcation highlights part 49 |
Patent application number | Title | Published |
20120035658 | Multiple Facet Joint Replacement - A prosthesis for the replacement of multiple diseased or traumatized spinal facets comprises a portion that replaces at least a bony portion of the facets to be replaced and where the prosthesis attaches to the vertebra in a manner that does not require attachment to, or abutment against, the lamina. Multiple configurations of the prosthesis provide for replacement of the two inferior facets, the two superior facets, a superior and inferior facet, or all four facets. A method of installing the prosthesis is provided that is comprised of the steps of resecting at least a portion of the facets that carry the diseased or traumatized spinal facets and attaching the prosthesis in a manner that does not require attachment or abutment against the lamina. | 2012-02-09 |
20120035659 | TRANSVERSE CONNECTOR - The present disclosure provides a transverse connector having first and second spinal rod connecting members disposed on opposing ends of a cross member. Each spinal rod connecting member is configured to connect to a spinal rod. The first and second spinal rod connecting members are configured for multidirectional articulation relative to the cross member. | 2012-02-09 |
20120035660 | Dynamic stabilization connecting member with pre-tensioned solid core - A dynamic longitudinal connecting member assembly includes an anchor member having an integral or otherwise fixed elongate core of circular or non-circular cross-section. The core is pre-tensioned and extends through at least one elastic spacer and at least one outer sleeve. The anchor member and the outer sleeve each attach to at least one bone anchor. In operation, the core is held in tension by the spacer. | 2012-02-09 |
20120035661 | MAINTENANCE FEATURE IN MAGNETIC IMPLANT - A distraction system includes a distraction rod having one end configured for affixation to at a first location on patient. The system further includes an adjustable portion configured for placement in the patient at a second location, the adjustable portion comprising a housing containing a magnetic assembly comprising a magnet, the magnetic assembly secured to a threaded element that interfaces with an opposing end of the distraction rod. The system includes a magnetically permeable member in proximity to the magnetic assembly and covering an arc of less than 360° of the adjustable portion. | 2012-02-09 |
20120035662 | ROD SCREW DYNAMIC IMPLANT FOR STABILIZING A VERTEBRAL COLUMN - The invention relates to an implant for supporting a vertebral column, including at least one attachment element ( | 2012-02-09 |
20120035663 | Dynamic stabilization medical implant assemblies and methods - Bone screw assemblies include longitudinal connecting members that provide for dynamic stabilization, some including non-uniform portions that are configured to flex, contract or expand. Composite longitudinal connecting members include longitudinal segments made from different materials having different flexibilities. Polyaxial bone screw assemblies include change-out receivers for cooperating with replacement longitudinal connecting members having a different flexibility. Bone screw shanks for cooperating with one or more open receivers include treatment or coating to provide biologically active interface with bone. | 2012-02-09 |
20120035664 | SYSTEM AND METHOD FOR INSERTION OF FLEXIBLE SPINAL STABILIZATION ELEMENT - Insertion of a spinal stabilization element into a patient generally includes positioning a cord within a sheath and inserting the sheath and cord through the patient's body along a path generally toward an anchor member. An advancement member may be mounted on the leading end of the cord to further facilitate this insertion. The sheath is then retracted to expose a first portion of the cord within the patient's body, and the first portion of the cord is moved into a desired position relative to the anchor member. After advancing a spacer over the sheath and cord, the sheath is retracted to expose a second portion of the cord. The second portion of the cord is then moved into a desired position relative to another anchor member such that the spacer is positioned between the two anchor members. | 2012-02-09 |
20120035665 | Orthopedic Plate Blocking Assembly - In an exemplary embodiment, the present invention provides an orthopedic plate blocking assembly that can be used for the fixation or fastening of an orthopedic plate to bone tissue. In particular, the present invention, in one embodiment, provides an orthopedic plate having a plurality of cavities where each cavity is configured and dimensioned to receive a bone anchoring member. The orthopedic plate further provides a blocking mechanism having a plurality of blocking members that block the bone anchoring members to prevent the bone anchoring members from “backing out” of cavities once the bone anchoring members are finally seated in the cavities. | 2012-02-09 |
20120035666 | Reduced Bone Fracture Fixation Device - Reduced bone fracture fixation devices and methods for using the same are provided. Aspects of the reduced bone fracture fixation devices include a body dimensioned to be positioned in a reduced bone fracture, wherein the body includes at least one tension element configured to exert a force on bone of the reduced bone fracture sufficient to maintain reduction of the reduced bone fracture. Aspects of the invention further include kits and methods of using and manufacturing the bone fracture fixation devices. The devices, kits and methods of the invention find use in a variety of applications, such as in applications in which it is desired to repair a reduced bone fracture. | 2012-02-09 |
20120035667 | LOCKING MECHANISMS FOR PIVOTING BONE ANCHORS - Bone anchors are provided that include a distal shaft for engaging bony structure of a vertebral body and a proximal post pivotably mounted at or near the proximal end of the shaft during implantation of the bone anchor. The bone anchors include a locking member that is engageable to the post and to the shaft to lock the post in a selected angular orientation relative to the shaft. | 2012-02-09 |
20120035668 | Derotation Apparatus For Treating Spinal Irregularities - Treatment of spinal irregularities, including, in one or more embodiments, derotation apparatus and systems that can be used to reduce the rotation of vertebral bodies. Derotation apparatus that may comprise a tube assembly comprising an inner sleeve and an outer sleeve disposed over the inner sleeve. The inner sleeve may have a distal end for attachment to an implant. The tube assembly may further comprise a handle assembly. The tube assembly may further comprise a ball joint assembly disposed between the tube assembly and the handle assembly. The ball joint assembly may comprise a ball joint configured for attachment to a coupling rod. The ball joint assembly further may comprise a reducing extension below the ball joint, the reducing extension being sized to fit in a central bore of the inner sleeve. Orthopedic fixation devices comprising a ball joint are also disclosed. | 2012-02-09 |
20120035669 | Polyaxial bone screw - A polyaxial bone screw assembly includes a threaded shank body having an upper capture structure, a head, a retaining ring and a nut. The external capture structure surface includes a threaded portion and a smooth portion; the smooth portion for slidably mating with the retaining ring and the threaded portion for rotatable attachment to the nut within a cavity of the head. The nut fixes the retaining ring to the shank and also provides a tool engagement formation for driving the shank body into bone. | 2012-02-09 |
20120035670 | Polyaxial bone anchors with pop-on shank, fully constrained friction fit retainer and lock and release insert - A polyaxial bone screw assembly includes a threaded shank body having an integral upper portion receivable in an integral receiver, the receiver having an upper channel for receiving a longitudinal connecting member and a lower cavity cooperating with a lower opening. The receiver can have crimp tabs, but is devoid of spring tabs and collet-like flexible structures. A down-loadable compression insert (some with lock and release feature), a down-loadable friction fit split retaining ring having super structure for temporary friction fit with an up-loadable shank upper portion cooperate 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. The shank and receiver once assembled cannot be disassembled. | 2012-02-09 |
20120035671 | Internal Joint Bracing System and Suture Anchoring Assembly Therefore - An internal bracing system is disclosed for stabilizing a joint such as the knee, shoulder, ankle or the like. The internal bracing system includes an extra-articular tension band mechanism and an anchor assembly therefore. The internal bracing system adds substantial control to unstable joints which is effective in limiting the pathological joint motions and internal slippage. The anchor anchoring assembly designed to affix a tethering device to various bony structures which form a joint, for the purpose of providing stability. The anchor assembly includes an anchor and a set screw. A double helix thread/chamber structure between the anchor and set screw securely holds the tether without binding. | 2012-02-09 |
20120035672 | CERAMIC CUTTING TEMPLATE - A cutting template or a cutting block, preferably to a cutting template or a cutting block for use in medical technology. | 2012-02-09 |
20120035673 | OSTEOARTHRITIS TREATMENT AND DEVICE - A method for treating arthritis of a joint includes identifying a bone lesion in a bone adjacent to the joint; and implanting in the bone a reinforcing member in or adjacent to the bone lesion. A kit for conducting the method includes: (a) at least one reinforcing member having a proximal face adapted to face the joint, a distal face adapted to face away from the joint, and a wedge-shaped edge adapted to pierce bone, wherein the at least one reinforcing member is planar and sterile; and (b) a container adapted to maintain the at least one reinforcing member sterile. Another kit includes: (a) a sterile fluid; (b) a syringe for injecting the fluid into a bone; (c) a curing agent adapted to cure the fluid to polymerize and/or cross-link; and (d) a container adapted to maintain the sterility of contents of the container. | 2012-02-09 |
20120035674 | SYSTEM FOR ANALYZING AND TREATING ABNORMALITY OF HUMAN AND ANIMAL TISSUES - A patient treatment unit for analyzing and treating abnormality of human or animal tissues, includes a display; a pulse generator circuit that outputs a sequence of electrical pulses at a pulse frequency, the electrical pulses having a pulse width, the pulse generator controlling the pulse frequency and the pulse width of the electrical pulses; a pair of probes for contacting a body of a patient and electrically coupled to the pulse generator; and a voltage and current sensing circuit that senses a voltage or a current via the probes when contacting the body of the patient. | 2012-02-09 |
20120035675 | EXTERNAL DEFIBRILLATOR WITH ADAPTIVE CPR DURATION - A method and apparatus for a defibrillating system is disclosed that monitors the patient during treatment and then uses the information it gathers to adjust treatment protocols during treatment based on the patient's response. The protocols may include adaptive rhythm analysis intervals, adaptive CPR intervals, and adaptive shock stacks. A method of operating a defibrillator may include the steps of: obtaining a data set on at least one physiological parameter of a patient in a first data gathering interval; performing an analysis of the data set; and determining a time interval between the analysis of the first data set and a second data set, or the duration of a CPR interval, or the number of shocks in a shock stack, based on the result of the analysis of the data set. | 2012-02-09 |
20120035676 | PULSE DETECTION USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 2012-02-09 |
20120035677 | DEFIBRILLATION SYSTEM AND CARDIAC DEFIBRILLATION METHOD - Provided is a defibrillation system including an electrode section that is attached to a heart and applies electrical energy to the heart, a defibrillator that generates the electrical energy on the basis of a predetermined defibrillation wave, and a lead that electrically connects the electrode section and the defibrillator. Further, the defibrillation wave includes a first wave generating first energy, a second wave generating second energy higher than the first energy of the first wave behind the first wave, and an application stop period formed between the first wave and the second wave. | 2012-02-09 |
20120035678 | PULSE DETECTION APPARATUS, SOFTWARE, AND METHODS USING PATIENT PHYSIOLOGICAL SIGNALS - The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided. | 2012-02-09 |
20120035679 | ACUTE MYOCARDIAL INFARCTION TREATMENT BY ELECTRICAL STIMULATION OF THE THORACIC AORTA - Apparatus and methods are described including identifying a subject as suffering from a condition selected from the group consisting of congestive heart failure, diastolic heart failure, acute myocardial infarction, and hypertension. In response to the identifying, an electrode is placed on the subject's aorta at an aortic site that is between a bifurcation of the aorta with the subject's left subclavian artery and a bifurcation of the aorta with the subject's fifth intercostal artery. The subject is treated by electrically stimulating the aortic site by driving a current into the aortic site, via the electrode. Other applications are also described. | 2012-02-09 |
20120035680 | Systems and Methods for Respiratory-Gated Auricular Vagal Afferent Nerve Stimulation - Neurostimulation is provided to afferent nerve fibers of an auricular vagal nerve of a patient. The neurostimulation is harmonized with the pulmonary activity of the patient. In one implementation, a neurostimulation is gated to a portion of the respiratory cycle. For example, the auricular vagal nerve may be stimulated at the end of exhalation. In another implementation, a stimulation regiment to multiple electrodes are harmonized with pre-selected triggers within the respiratory cycle to achieve selective stimulation and/or bilateral stimulation. | 2012-02-09 |
20120035681 | SYSTEMS AND METHODS FOR ESTIMATING LEFT ATRIAL PRESSURE (LAP) IN PATIENTS WITH ACUTE MITRAL VALVE REGURGITATION FOR USE BY AN IMPLANTABLE MEDICAL DEVICE - Various techniques are provided for use with an implantable medical device for estimating cardiac pressure within a patient based on admittance (or related electrical values such as impedance or conductance) that takes into account the presence of acute MR within the patient. Briefly, the device detects an indication of acute MR, if occurring within the patient. The device also applies electrical fields to tissues of the patient and measures electrical parameters influenced by the electrical field, such as admittance, impedance or conductance. The device then estimates cardiac pressure within the patient based on the measured electrical parameter and the indication of acute MR. In one example, different linear correlation functions are used to convert admittance values to left atrial pressure (LAP) values depending upon the presence or absence of acute MR within the patient. | 2012-02-09 |
20120035682 | SYSTEM AND METHOD FOR TESTING NEURAL STIMULATION THRESHOLD - Various system embodiments comprise a neural stimulator, a premature ventricular contraction (PVC) event detector, a heart rate detector, an analyzer, and a controller. The neural stimulator is adapted to generate a stimulation signal adapted to stimulate an autonomic neural target. The analyzer is adapted to, in response to a PVC event signal from the PVC event detector, generate an autonomic balance indicator (ABI) as a function of pre-PVC heart rate data and post-PVC heart rate data. Other aspects and embodiments are provided herein. | 2012-02-09 |
20120035683 | METHOD FOR TREATING DEGENERATIVE DISC DISEASE USING NONINVASIVE CAPACITIVELY COUPLED ELECTRICAL STIMULATION DEVICE - A method for treatment of degenerative disc disease using capacitively coupled electrical stimulation. In one embodiment, a subject diagnosed as having degenerative disc disease is treated by placing first and second electrodes on the subject's body at the site of an identified disc in a state of degenerative disc disease, and applying an electric field to the identified disc via the first and second electrodes with the intent to treat the degenerative disc disease. The electric field is created with an electrical signal having a frequency within a range of 20 to 100 kHz and having a symmetrical waveform with an amplitude within a range of 0.1 to 20 volts peak-to-peak, preferably a frequency of approximately 60 kHz and an amplitude of approximately 5 volts peak-to-peak. | 2012-02-09 |
20120035684 | Multiplexed, Multi-Electrode Neurostimulation Devices with Integrated Circuits Having Integrated Electrodes - Implantable stimulation devices are provided. Aspects of the devices include a multiplexed multi-electrode component configured for neural stimulation. The multiplexed multi-electrode component includes two or more individually addressable satellite electrode structures electrically coupled to a common conductor. The satellite structures include a hermetically sealed integrated control circuit operatively coupled to one or more electrodes. Also provided are methods of manufacturing wherein the application of laser welding is avoided in forming the satellite electrode structures and an integrated control circuit thereof is thereby shielded from mechanical stress during satellite manufacture. Additionally provided are systems that include the devices of the invention, as well as methods of using the systems and devices in a variety of different applications. | 2012-02-09 |
20120035685 | USER INTERFACE SYSTEM FOR USE WITH MULTIPOLAR PACING LEADS - An interactive representation of electrostimulation electrodes or vectors can be provided, such as for configuring combinations of electrostimulation electrodes. In an example, electrodes or test parameters can be presented graphically or in a table. A user interface can be configured to receive user-input designating electrode combinations or vectors for test or for use in programming an implantable or ambulatory medical device. The interface can be used to indicate suggested electrode combinations or vectors in response to a first selection of an electrode. Tests can be performed on electrode combinations and vectors, and the results of the tests can be presented to a user using the interactive representation. In an example, test results can be analyzed by a processor and optionally used to program an implantable or ambulatory medical device. | 2012-02-09 |
20120035686 | FAIL-SAFE PROGRAMMING FOR IMPLANTABLE MEDICAL DEVICE - In general, the invention is directed to a system with a fail-safe mode for remote programming of medical devices, such as implantable medical devices (IMDs). During a remote programming session, an adverse event, such as a programming session failure, may prevent proper completion of a programming or result in improper programming due to data corruption or other factors. If a programming session is not completed correctly, the IMD is susceptible to improper operation, possibly exposing a patient to delivery of unnecessary or inappropriate therapies. A fail-safe mode reduces the likelihood of improper operation following a programming session failure. The fail-safe mode defines one or more fail-safe operations designed to preserve proper operation of the IMD. In some embodiments, the fail-safe operations include notifying a person concerning the failure of the programming session, modifying programming parameters within the implantable medical device, and delivering a therapy to a patient. | 2012-02-09 |
20120035687 | IMPLANTABLE ELECTRICAL STIMULATOR - Disclosed herein is an implantable electrical stimulator which includes two stimulating electrodes, a system-on-chip and an inductive coil. The system-on-chip can apply electric stimulation to the dorsal root ganglion via the stimulating electrodes. An external power supply can wirelessly charge the system-on-chip through the inductive coil. | 2012-02-09 |
20120035688 | APPARATUS FOR LOCALISED INVASIVE SKIN TREATMENT USING ELECTROMAGNETIC RADIATION - Skin tissue measurement/treatment apparatus ( | 2012-02-09 |
20120035689 | HEAT AND LIGHT-EMITTING PAD - An application for a heat and light emitting pad has an array of light and heat emitting devices such as LEDS mounted on a circuit board and held within a sponge material. A controller provides a controlled amount of power to the LEDS such that the LEDS emit a therapeutic amount of heat and light for the treatment of pain. The heat and light emitting pad is a thin sheet for insertion between a person and a surface on which that person rests. | 2012-02-09 |
20120035690 | WORN HEAT AND LIGHT-EMITTING DEVICE - An application for a wearable heat and light emitting device has an array of light and heat emitting devices such as LEDS mounted on a circuit board and held within a sponge material. The array of LEDs is held against a portion of a person's body by a fastening device such as a belt. A controller provides a controlled amount of power to the LEDS such that the LEDS emit a therapeutic amount of heat and light for the treatment of pain. The heat and light emitting devices form a thin sheet for wearing against a portion of a person's body that experiences pain. | 2012-02-09 |
20120035691 | SYSTEM AND METHOD FOR SECURING A LEAD IN A VESSEL - A two-part system for securing and stabilizing a lead at a location within a patient's internal jugular vein adjacent a region of the vagus nerve to be stimulated is described. The two-part system includes a lead and a stent-like fixation member that is provided separate from the lead. The stent-like fixation member is used to secure an electrode region of the lead at a location within the internal jugular vein adjacent the vagus nerve. The stent-like fixation member urges the electrode region of the lead against the vessel walls of the internal jugular vein such that at least one electrode is oriented in a direction towards the vagus nerve. In one example, the stent-like fixation member includes a channel sized to receive and retain a portion of the lead therein. | 2012-02-09 |
20120035692 | IMPLANTABLE MEDICAL ANCHOR - There is disclosed various embodiments of an implantable anchor for permanently anchoring a medical lead or catheter. For instance, there is disclosed an implantable anchor including a body having a longitudinal lumen defined therein, wherein the longitudinal lumen is sized to accept a portion of the medical lead or catheter, a bending mechanism coupled to the body for bending the lead to a predetermined angle within the body, and a retaining mechanism for maintaining the predetermined angle of the bent lead within the body. | 2012-02-09 |
20120035693 | IMPLANTABLE MRI COMPATIBLE MEDICAL LEAD - A medical implantable lead is adapted to be implanted into a human or animal body for monitoring and/or controlling of an organ inside the body, and has in a distal end, a combined fixation means and electrode member in form of a helix, which is rotatable in relation to the lead and extendable out from the distal end by rotation of a tubular torque transferring member. The helix is electrically connected to a connector in the proximal end by at least one electrically conducting wire, which is formed as an electrically conducting coil, which is separate from the tubular torque transferring member and that includes one or more individual wires each having an electrically conducting wire core and a surrounding electrically insulating layer. The tubular torque transferring member has no electrically conducting function to or from the helix. The lead is arranged such that the electrical connection between the helix and the conducting wire is always maintained regardless of the rotational position of the helix while no electrical connection is present between the helix and the tubular torque transferring member although the helix is rotatable by the tubular torque transferring member. | 2012-02-09 |
20120035694 | GROUNDING OF A SHIELD WITHIN AN IMPLANTABLE MEDICAL LEAD - Grounding of a shield that is located in an implantable medical lead may be done in many ways. The shield may be grounded directly to tissue from the lead body at one or more points along the lead body. The pathway for grounding may be a direct current pathway or be capacitively coupled. The pathway for grounding may utilize an exposed or nearly exposed shield at one or more points along the lead body. A jacket forming the lead body may have an outer layer removed at these points to provide the RF pathway to ground. Alternatively, the jacket may be doped with conductive particles at these points. Metal conductors such as ring electrodes and/or lead anchors may be attached to the lead at one or more points to provide the RF pathway to ground. | 2012-02-09 |
20120035695 | GROUNDING OF A SHIELD WITHIN AN IMPLANTABLE MEDICAL LEAD - Grounding of a shield that is located in an implantable medical lead may be done in many ways. The ground pathway may couple to the shield at a point that is outside of a header of an implantable medical device to which the implantable medical lead is attached. The ground pathway may couple to the shield at a point that is within the header of the implantable medical device. The ground pathway may terminate at the metal can of the implantable medical device. As another option, the ground pathway may terminate at a ground plate that is mounted to the header. The ground pathway may be direct current coupled from the shield to the can or ground plate. Alternatively, the ground pathway may include one or more capacitive couplings that provide a pathway for induced radio frequency current. | 2012-02-09 |
20120035696 | TERMINATION OF A SHIELD WITHIN AN IMPLANTABLE MEDICAL LEAD - A shield located within an implantable medical lead may be terminated in various ways. The shield may be terminated by butt, scarf, lap, or other joints between insulation layers surrounding the lead and an insulation extension. For lap joints, a portion of an outer insulation layer may be removed and a replacement outer insulation layer is positioned in place of the removed outer insulation layer, where the replacement layer extends beyond an inner insulation layer and the shield. The replacement layer may also lap onto a portion of the insulation extension. Barbs may be located between the replacement layer and the inner insulation layer or the insulation extension. The shield wires have ends at the termination point that may be folded over individually or may be capped with a ring located within one of the insulation layers of the jacket. | 2012-02-09 |
20120035697 | SHIELDED IMPLANTABLE MEDICAL LEAD WITH GUARDED TERMINATION - Implantable medical leads include a shield that is guarded at a termination by having a first portion and second portion of the shield, where the first portion is between a termination of the shield at the second portion and an inner insulation layer surrounding the filars. The first portion may reduce the coupling of RF energy from the termination of the shield at the second portion to the filars. The first and second portions may be part of a continuous shield, where the first and second portions are separated by an inversion of the shield. The first and second portions may instead be separate pieces. The first portion may be noninverted residing between the termination at the second portion and inner layers, or the first portion may be inverted to create first and second sub-portions. The shield termination at the second portion is between the first and second sub-portions. | 2012-02-09 |
20120035698 | CAPACITOR AND INDUCTOR ELEMENTS PHYSICALLY DISPOSED IN SERIES WHOSE LUMPED PARAMETERS ARE ELECTRICALLY CONNECTED IN PARALLEL TO FORM A BANDSTOP FILTER - One or more inductors and one or more capacitors are physically disposed relative to one another in series and are electrically connected to one another in parallel to form a bandstop filter. Chip inductors and chip capacitors having spaced apart conductive terminals are physically arranged in end-to-end abutting relation to minimize electrical potential between adjacent conductive terminals. The bandstop filter may be hermetically sealed within a biocompatible container for use with an implantable lead or electrode of a medical device. The values of the inductors and the capacitors are selected such that the bandstop filter is resonant at one or more selected frequencies, such as an MRI pulsed frequency. | 2012-02-09 |
20120035699 | METHOD AND APPARATUS FOR FIXATING AN IMPLANTABLE MEDICAL DEVICE - A fixation mechanism coupled to an implantable device body extends from a proximal portion of the body to a distal portion of the body and includes a fixation element and a push tube segment. A push tube segment of the mechanism extends proximally from the fixation mechanism to the proximal portion of the body and is adapted to deploy the mechanism. | 2012-02-09 |
20120035700 | STENT DELIVERY SYSTEM - A drainage stent delivery system including an elongate shaft of a medial device, a drainage catheter or stent, and a retention mechanism for selectively retaining the drainage stent on the elongate shaft. The tubular stent is positioned on and surrounding the elongate shaft. The elongate shaft includes a distal tip portion which is deflectable from a first position to a second position, the distal tip portion of the elongate shaft being biased toward the first position. Deflecting the distal tip portion of the elongate shaft from the first position to the second position moves the distal tip portion toward the central longitudinal axis of the tubular stent to allow the stent to be decoupled from the elongate shaft. | 2012-02-09 |
20120035701 | STENT STRUT APPOSITIONER - The teachings provided herein are generally directed to a method, device and system for use in reducing, inhibiting, or correcting a malapposed intraluminal device. An example of such an intraluminal device is a stent and, in some embodiments, the intraluminal device can be any device known to one of skill, the implementation of which might benefit from the teachings provided herein. In some embodiments, the intraluminal device is a cardiac stent. | 2012-02-09 |
20120035702 | STENT FOR VALVE REPLACEMENT - An expandable stent ( | 2012-02-09 |
20120035703 | Truncated Conical Heart Valve Stent with Anchoring Threads and Methods of Use - A heart valve stent and methods of use thereof, such stent having a heart valve implant and several proximally disposed tissue anchors, also comprising a plurality of anchoring threads, each with a proximate end fastened to the stent or valve and a distal end attached to tissue within a heart chamber to provide tension between the heart chamber tissue and the stent. | 2012-02-09 |
20120035704 | PROCESS FOR LOADING A STENT ONTO A STENT DELIVERY SYSTEM - The present invention relates to a stent delivery system and a process for mounting a stent onto a delivery system. More specifically, the present invention relates to a method of loading a stent onto a balloon and mounting the stent balloon assembly onto a catheter. The premounting of the stent onto the balloon subassembly allows the stent to be crimped in a way that the crimping recoil can be compensated and stent retention is kept at a maximum. | 2012-02-09 |
20120035705 | DEPLOYMENT DEVICE FOR PLACEMENT OF MULTIPLE INTRALUMINAL SURGICAL STAPLES - A system for delivering a surgical staple can include various components. The system may include an elongate body with a proximal end, a distal end, and a plurality of delivery platforms disposed adjacent the distal end. A sheath can move relative to the elongate body from a first position in which the distal end of the sheath is disposed distally of a distal-most distal delivery platform to a second position in which the distal end of the sheath is disposed proximally of at least one delivery platform. A plurality of intravascular tacks can be within the system with each disposed about a corresponding delivery platform. | 2012-02-09 |
20120035706 | BLOOD PERFUSION DEVICE DELIVERY SYSTEM - A delivery system deploys a prosthesis for open surgical repair of a body vessel. The system includes a sleeve to retain segments of a prosthesis in a compressed configuration and retraction members. The sleeve has outer segments associated with each end of the prosthesis. Retraction of the retraction members removes the outer segments of the sleeve from the prosthesis outer ends to allow for expansion of the outer ends of the prosthesis in an outside-in direction. The system can include a handle and an actuation member movably attached to the handle. The actuation member is coupled to the sleeve outer segments so that movement of the actuation member corresponds to removal of the sleeve. The system can include elements to retain the sleeve outer segments to the actuation member and to redirect the retraction members to a direction different from the axis of the prosthesis. | 2012-02-09 |
20120035707 | METHODS OF USING IMPLANTABLE MEDICAL DEVICE DETACHMENT SYSTEM - Implantable medical device detachment methods are provided using a carrier member having a compressible portion at a distal end thereof. The compressible portion is moved to a compressed condition to allow an engagement member of the system to releasably engage an implantable device, such as an embolic coil. The carrier member and associated implantable device are fed through a body vessel to a target location, where the device is disengaged from the engagement member. The compressible portion then moves from the compressed condition to an elongated condition to completely separate the implantable device from the engagement member. | 2012-02-09 |
20120035708 | BLOOD PERFUSION DEVICE - A perfusion device and a delivery system for repair of a damaged portion of a body vessel. Perfusion device can include a tubular body that is self-expandable, having a proximal portion, a distal portion, and an intermediate portion. One or more series of barbs can be disposed circumferentially along the intermediate portion. Barbs are capable of penetrating into the tunica intima and tunica media of said vessel wall upon insertion of said device into said body vessel, and not into said tunica adventitia. A graft can be associated with the tubular body. Graft has a proximal end and a distal end, and preferably extends entirely along a luminal wall of the tubular body. Graft may also extend along an exterior surface of the tubular body at the proximal and distal portions. A remodelable covering can be applied along the intermediate portion. Delivery devices for the perfusion implant and methods of delivering the perfusion implant are also provided. | 2012-02-09 |
20120035709 | ENDOPROSTHESIS HAVING FOOT EXTENSIONS - Endoprosthesis for delivery in a body lumen is provided. The endoprosthesis includes an annular element defined by a set of interconnected strut members, each strut member including a first end and a second end. The first end of selected pairs of circumferentially-adjacent strut members of the annular element are interconnected to define apices proximate a first longitudinal side of the annular element and the second end of selected pairs circumferentially-adjacent strut members are interconnected to define apices proximate a second longitudinal side of the annular element. At least one of the selected pairs of circumferentially-adjacent strut members has a modulator disposed proximate the apex defined there between, the modulator having a first mode to allow expansion of the annular element from an unexpanded configuration toward an expanded configuration and a second mode to resist contraction of the annular element from the expanded configuration toward the unexpanded configuration. | 2012-02-09 |
20120035710 | RING STENT - A stent arrangement which has at least a first ring ( | 2012-02-09 |
20120035711 | ENHANCING PERFUSION BY CONTRACTION - Apparatus and methods are described including a mechanical support element that is placed inside a first vein of a subject. At least one electrode disposed on the mechanical support element is placed inside the first vein, in a vicinity of a site upstream of a bifurcation with a second vein of the subject. A control unit enhances downstream blood flow from the first vein by driving the at least one electrode to divert blood downstream into the second vein by constricting the first vein at the upstream site, by driving the at least one electrode to apply a current to the vicinity of the site. The mechanical support element prevents the first vein from collapsing by providing mechanical support to the vein. Other embodiments are also described. | 2012-02-09 |
20120035712 | METHOD AND APPARATUS FOR TRICUSPID VALVE REPAIR USING TENSION - Apparatus is provided, including a radially-expandable percutaneous implant, a tissue anchor, and a connecting element shaped so as to provide an annular loop surrounding a proximal portion of the tissue anchor in a manner which enables rotation of the anchor about a central longitudinal axis thereof when surrounded by the annular loop. The apparatus also includes a flexible longitudinal member coupled at a first portion thereof to at least a portion of the percutaneous implant and at a second portion to the connecting element. The annular loop of the connecting element facilitates rotation of the tissue anchor about the central longitudinal axis such that the anchor can rotate about the central longitudinal axis with respect to the annular loop, the flexible longitudinal member, and the percutaneous implant. Other applications are also described. | 2012-02-09 |
20120035713 | Truncated Cone Heart Valve Stent - A heart valve stent having a section with a heart valve implant and several proximally disposed tissue anchors, also comprising a plurality of anchoring threats, each with a proximate end fastened to the stent or valve and a distal end attached to tissue within a heart chamber to provide tension between the heart chamber tissue and the stent. | 2012-02-09 |
20120035714 | Stent Graft Having A Marker And A Reinforcing And Marker Ring - A reinforcing and marker ring for a stent graft is disclosed. The reinforcing and marker ring comprises a plurality of turns of a substantially inextensible resilient wire in a circular shape and terminal ends at each end of the wire. The terminal ends each comprise a loop, each loop attachable to a stent graft having an opening or a fenestration so as to substantially lock a peripheral length of the circular shape. A marker winding is wound helically around the reinforcing wire, the marker winding being viewable on an image display system employing electromagnetic radiation so as to indicate the location of a periphery of the fenestration. The circular shape of the resilient wire, with the marker winding wound around it, is collapsible under radial pressure to form a squashed circular shape for loading into a delivery device, the squashed circular shape self-expandable back to a substantially circular shape upon release from the delivery device. The marker winding defines a curved passageway around the resilient wire of the reinforcing ring, the curved passageway having an internal diameter D, wherein the marker winding is helically wound with a pitch providing at least one winding per length D along the reinforcing wire of the reinforcing ring. The marker winding may be a radiopaque gold wire wound around a nitinol reinforcing wire. | 2012-02-09 |
20120035715 | Tracheal Stent With Longitudinal Ribs to Minimize Stent Movement, Coughing and Halitosis - A tracheal stent is an expandable tubular member having a proximal end, a distal end, an inner surface, and an outer surface. Circumferentially adjacent surface protrusions extend outwardly from the outer surface of the expandable tubular member. These surface protrusions have an outer surface, a first lateral surface and a second lateral surface. When the tracheal stent is deployed, the outer surface of the surface protrusion applies a radial force to a wall of the trachea to remove an airway constriction. | 2012-02-09 |
20120035716 | POLYLACTIDE-COATED IMPLANT COMPOSED OF A BIOCORRODIBLE MAGNESIUM ALLOY - Some invention embodiments relate to an implant having a base body composed of a biocorrodible magnesium alloy and a polylactide coating. The implant is characterized in that the coating contains seed crystals and/or lipophilic substances as additives. | 2012-02-09 |
20120035717 | Catheter Assembly with Valve Crimping Accessories - Valve delivery catheter assemblies including components that limit trauma to the expanded prosthetic valve and body channels as the distal tip of the catheter is withdrawn through the expanded valve and thereafter from the body. In one embodiment, a catheter assembly according to the present invention includes a handle assembly, an introducer sheath, and a distal tip assembly. The handle assembly can include a fixed main handle and two or more rotating handles that allow a user to control the distal tip assembly of the catheter. A valve retaining mechanism can be included to assist in retaining the prosthetic valve prior to deployment. Each control knob on the handle assembly controls a portion of the components on the distal tip of the catheter by allowing for precise manipulation of various delivery shafts. Each delivery shaft extends from the handle assembly to respective positions towards the distal end of the catheter. | 2012-02-09 |
20120035718 | DEVICES, SYSTEMS, AND METHODS FOR RESHAPING A HEART VALVE ANNULUS - Implants or systems of implants and methods apply a selected force vector or a selected combination of force vectors within or across the left atrium, which allow mitral valve leaflets to better coapt. The implants or systems of implants and methods make possible rapid deployment, facile endovascular delivery, and full intra-atrial retrievability. The implants or systems of implants and methods also make use of strong fluoroscopic landmarks. The implants or systems of implants and methods make use of an adjustable implant and a fixed length implant. The implants or systems of implants and methods may also utilize a bridge stop to secure the implant, and the methods of implantation employ various tools. | 2012-02-09 |
20120035719 | Prosthetic Heart Valves, Support Structures and Systems and Methods for Implanting the Same - Prosthetic valves and their component parts are described, as are prosthetic valve delivery devices and methods for their use. The prosthetic valves are particularly adapted for use in percutaneous aortic valve replacement procedures. The delivery devices are particularly adapted for use in minimally invasive surgical procedures. | 2012-02-09 |
20120035720 | Method of Cutting Tissue Using a Laser - A prosthetic heart valve assembly comprises a plurality of leaflets configured to replace the function of a native heart valve. Each leaflet comprises laminar pericardium tissue. Each leaflet has a coaptation edge formed by laser cutting. The tissue layers of each leaflet are fused together along an entire length of the coaptation edge, and tissue adjacent each coaptation edge does not have significant thermal energy damage. | 2012-02-09 |
20120035721 | TEMPORARY SUB-VALVULAR CHECK VALVE - A temporary subvalvular check valve has a collar and an expandable seal structure connected by pivotable struts that together support flexible leaflets. The check valve can be introduced along a tool shaft and positioned in a chamber or vasculature by expanding the seal structure against an adjacent wall. Cardiac function is augmented during valve procedures, such as valve excision, valve implantation, or valve leaflet replacement, by placing the temporary check valve just upstream of the valve being treated. The temporary check valve is collapsible so that it can be inserted through a small incision or port in the apex of the heart or through the aorta, into the ventricular cavity. Such a system thus does not require arrest or pacing of the heart and will allow such valve repair or replacement procedures to be done without concern for time or compromise to the patients' physiology. | 2012-02-09 |
20120035722 | Mitral Prosthesis and Methods for Implantation - A mitral valve prosthesis and methods for implanting the prosthesis transapically (i.e., through the apex of the heart), transatrially (i.e., through the left atrium of the heart), and transseptally (i.e., through the septum of the heart). The prosthesis generally includes a self-expanding frame and two or more support arms. A valve prosthesis is sutured to the self-expanding frame. Each support arm corresponds to a native mitral valve leaflet. At least one support arm immobilizes the native leaflets, and holds the native leaflets close to the main frame. | 2012-02-09 |
20120035723 | PROSTHESIS FOR MITRAL ANNULOPLASTY - A prosthesis ( | 2012-02-09 |
20120035724 | Accommodating intraocular lens and methods of use - An accommodating intraocular lens, for use in an eye, is made from flexible, optionally elastic, bio-compatible lens body material surrounding a s closed and sealed lens cavity which is filled with bio-compatible optical liquid, optionally a gel. The optical liquid has a refractive index sufficiently high to, in cooperation with the ciliary muscle, focus light, incident on the eye, on the retina, and to provide accommodation. The curvature of the front surface of the lens is deformable, by the pressure expressed by the ciliary body during the to accommodative effort, thus to change the radius of curvature of the anterior body member and/or the posterior body member, thus providing smooth focusing, including from far distance in the relaxed state to near distance of less than 50 centimeters in the accommodative state. | 2012-02-09 |
20120035725 | RETINAL PROSTHESIS TECHNIQUES - Apparatus is provided including an external device including, a mount, which is placed in front of an eye of a subject. A power source is coupled to the mount and emits energy toward the eye. An intraocular device is implanted entirely in the subject's eye, and includes a control unit, a plurality of stimulating electrodes, and an energy receiver, which receives the energy from the power source and generates a voltage drop in response thereto. A plurality of photosensors detect photons and generate a signal in response thereto. Driving circuitry is coupled to the energy receiver and to the photosensors, and drives the electrodes to apply electrical charges to a retina in response to the signals from the photosensors. The external device modulates the emitted energy, and the control unit demodulates the modulated energy to regulate an operation parameter of the intraocular device. Other embodiments are also described. | 2012-02-09 |
20120035726 | RETINAL PROSTHESIS TECHNIQUES - Apparatus for use with an external non-visible light source is provided. The apparatus comprises an intraocular device configured for implantation in a human eye, and comprising an energy receiver. The energy receiver is configured to receive light emitted from the external non-visible light source, and extract energy from the emitted light for powering the intraocular device. The intraocular device is configured to regulate a parameter of operation of the intraocular device based on a modulation of the light emitted by the external non-visible light source and received by the energy receiver. Other embodiments are also described. | 2012-02-09 |
20120035727 | SURGICAL IMPLANT DEVICE FOR THE TRANSLATION AND FUSION OF A FACET JOINT OF THE SPINE - The present invention provides, among other things, a surgical device for the translation/distraction and subsequent stabilization/fusion of a facet joint of a spine, including: a post that is selectively disposed partially between articulating surfaces of the facet joint; and a keel structure that is selectively disposed about the post and impacted into the articulating surfaces of the facet joint, wherein, when the keel structure is selectively rotated about the post, the articulating surfaces of the facet joint are moved with respect to one another. | 2012-02-09 |
20120035728 | Prothesis For the Replacement of a Posterior Element of a Vertebra - Prosthetic replacement for a posterior element of a vertebra comprising portions that replace the natural lamina and the four natural facets. The prosthetic replacement may also include portions that replace one or more of the natural spinous process and the two natural transverse processes. If desired, the prosthesis replacement may also replace the natural pedicles. A method for replacing a posterior element of a vertebra is also provided. | 2012-02-09 |
20120035729 | Expandable Fusion Device and Method of Installation Thereof - The present invention provides an expandable fusion device capable of being installed inside an intervertebral disc space to maintain normal disc spacing and restore spinal stability, thereby facilitating an intervertebral fusion. In one embodiment, the fusion device includes a body portion, a first endplate, and a second endplate, the first and second endplates capable of being moved in a direction away from the body portion into an expanded configuration or capable of being moved towards the body portion into an unexpanded configuration. The fusion device is capable of being deployed and installed in both configurations. | 2012-02-09 |
20120035730 | MINIMALLY-INVASIVE RETROPERITONEAL LATERAL APPROACH FOR SPINAL SURGERY - A method is disclosed for introducing a spinal disc implant into an intervertebral space of a subject. The subject is placed in a lateral position, and the anterior face of the spinal disc intervertebral space is accessed, between the L5 and S1 vertebrae, from an anterior and lateral retroperitoneal approach. An operative corridor to the anterior face of the spinal disc space is established by introducing a retractor instrument anterolaterally to the spinal disc space between the anterior superior iliac spine and the anterior inferior iliac spine. The damaged spinal disc contents are removed from the intervertebral space through the operative corridor, and the implant is advanced into the intervertebral space at an oblique angle and pivoted to position the implant substantially laterally within the intervertebral space. Elongated retractor and insertion instruments, as well as a modified disc implant, are also disclosed for carrying out the method. | 2012-02-09 |
20120035731 | INTERVERTEBRAL DISC PROSTHESIS - The invention relates to an intervertebral disc prosthesis ( | 2012-02-09 |
20120035732 | INTERVERTEBRAL PROSTHETIC DISC - A prosthetic disc for insertion between adjacent vertebrae includes upper and lower plates, a core disposed between the plates, and at least one projection extending from at least one of the upper and lower curved surfaces of the core into at least one recess of one of the inner surfaces of the plates. The recess is oversize with respect to the projection to allow sliding movement of the plate over the core while retaining the core between the plates during such sliding movement. The projection(s) may include a rod extending through an axial hole in the core, multiple surface features of the core, or the like. | 2012-02-09 |
20120035733 | PROSTHETIC HAVING A MODULAR SOFT TISSUE FIXATION MECHANISM - A method and apparatus for coupling soft tissue to a prosthetic is disclosed. Soft tissue attachment pads having porous metal attachment regions and suture accepting holes are selectively positioned onto an implantable prosthetic to provide coupling locations. | 2012-02-09 |
20120035734 | Intracorporeal Component for a Percutaneous Device - An intracorporeal portion of a percutaneous device for a joint disarticulation prosthesis or joint replacement prosthesis, the intracorporeal portion having an extracorporeal portion or having means for rigidly coupling directly to an extracorporeal portion, the extracorporeal portion being for location exterior to the skin, the intracorporeal portion having an articulating component for articulating with an articulating surface, wherein the articulating component is intracorporeal when installed in a human or animal subject. | 2012-02-09 |
20120035735 | TIBIAL PROSTHESIS - A tibial prosthesis, and, particularly, a fixed bearing tibial prosthesis has a two-pronged securement mechanism. The securement mechanism may or may not be angled. Advantageously, the securement mechanism, working alone or in cooperation with other securement features, minimizes micromotion between the tibial tray and tibial bearing component. | 2012-02-09 |
20120035736 | Tibial component - A tibial knee joint prosthesis for attachment to a suitably prepared tibial bone, providing bearing portions in the lateral and medial compartments. The lateral and medial bearing surfaces of the component are inclined at different angles in the anterior to posterior direction of the knee, so that when mounted to the tibia, the lateral bearing surface of the prosthesis is higher than the medial bearing surface to the posterior side of the knee. In this way the lateral ligament is tightened progressively more than the medial ligament as the knee moves from extension to flexion, resulting in increased stability in the lateral compartment. | 2012-02-09 |
20120035737 | TIBIAL PROSTHESIS - A tibial prosthesis has a bearing component configured for an anterior-medial insertion, which advantageously avoids the extensor mechanism of the knee. A tibial tray may include a banana-shaped boss that corresponds to a notch formed in the bearing component. After the bearing component is inserted along the anterior-medial path, the boss is received within the notch by rotating the bearing component with respect to the tibial tray. This rotation seat the bearing component upon the tibial tray in the manner of a fixed-bearing prosthesis. Alternatively, the boss and notch may define angled central axes which allow straight anterior-medial insertion of the bearing component and locking engagement to the tibial tray. | 2012-02-09 |
20120035738 | INTRAVITREOUS SELF ADAPTIVE STENT - Disclosed herein are devices, methods and kits for a stent for treating an eye, comprising a flexible material, wherein the stent is self adaptive to a dimension of a vitreous cavity in the eye. | 2012-02-09 |
20120035739 | DESIGNED SURFACES FOR USE IN MEDICAL IMPLANTS OR INSTRUMENTS - A medical implant device or component thereof comprising a metal substrate and a coating layer structure provided on the substrate. The coating layer structure comprises an outermost layer of a ceramic material. A bonding structure is deposited between the metal substrate and the coating layer structure. The bonding structure comprises a chromium rich layer, which is deposited onto the metal substrate surface and has a higher concentration of chromium than the metal substrate, as well as a gradient layer having a composition gradient from the chromium rich layer towards the surface of the device providing increasing proportions of a gradient material which has structural correspondence with the layer of the coating layer structure that is most adjacent to the bonding structure. | 2012-02-09 |
20120035740 | BIODEGRADABLE IMPLANT AND METHOD FOR MANUFACTURING SAME - This invention relates to a biodegradable implant including magnesium, wherein the magnesium contains, as impurities, (i) manganese (Mn); and (ii) one selected from the group consisting of iron (Fe), nickel (Ni) and mixtures of iron (Fe) and nickel (Ni), wherein the impurities satisfy the following condition: 0(i)≦5, and an amount of the impurities is 1 part by weight or less but exceeding 0 parts by weight based on 100 parts by weight of the magnesium, and to a method of manufacturing the same. | 2012-02-09 |
20120035741 | SELF-EXPANDABLE BIOPOLYMER-MINERAL COMPOSITE - A compressed implant composite for repairing mineralized tissue. The compressed implant composite includes a matrix formed of biopolymeric fibers and a plurality of calcium- and/or silicate-based mineral particles dispersed in the matrix. The matrix constitutes 4 to 80% by weight and the mineral particles constitute 20 to 96% by weight of the composite. The composite is free of soluble collagen and is expandable to a volume 2 to 100 times of its compressed volume (e.g., upon absorption of water). Also disclosed are methods of preparing the above-described composite. | 2012-02-09 |
20120035742 | Methods, Devices and Systems for Bone Tissue Engineering Using a Bioreactor - An anatomically-shaped, human bone graft may be cultivated ex vivo using a bioreactor capable of perfusing large complex porous scaffolds. Scaffolds derived from image-based modeling of a target are seeded with human mesenchymal stem cells and cultivated. A bioreactor configured to house complex three-dimensional scaffold geometries provides controlled flow for perfusion of the cells. Dense uniform cellular growth can be attained throughout the entire scaffold as a result of the medium perfusion. In an embodiment, the bioreactor has a mold into which perfusion medium is pumped under pressure and multiple ports through which the medium exits the mold. | 2012-02-09 |
20120035743 | AMNION AND CHORION CONSTRUCTS AND USES THEREOF IN MINIMALLY INVASIVE SURGERIES - A construct for use in a minimally invasive surgery is described. The construct contains an allograft having at least one layer of human amnion and chorion tissues, and is adapted for insertion into a small incision or a cannula employed in the minimally invasive surgery for access to the surgical site. The allograft has a shape appropriate for covering the surgical site. Methods of preparing the construct and using it in a minimally invasive surgery are also described. The products and methods improve the performance of the minimally invasive surgery, e.g., by reducing adhesions, scar formation while also reducing inflammation and risk of post-operative infection. | 2012-02-09 |
20120035744 | AMNION AND CHORION CONSTRUCTS AND USES THEREOF IN JOINT REPAIR - A construct for use in a surgical repair of a damaged or inflamed joint is described. The construct contains an allograft having at least one layer of human amnion and chorion tissues, and is adapted for enclosing a damaged or inflamed joint or for covering or replacing a damaged or inflamed joint sheath during the surgical repair. Methods of preparing the construct and using it in a surgical repair of a damaged or inflamed joint are also described. The products and methods improve the performance of the joint surgery, e.g., by reducing inflammation, inhibiting fibrosis, scarring, fibroblast proliferation and post-operative infection while also promoting more rapid healing of damaged or traumatized joints. | 2012-02-09 |
20120035745 | PROCESSING INFORMATION ACQUISITION SYSTEM IN PROCESSING MACHINE SUPPLYING PROCESSING POINT WITH ENERGY OR MATERIAL - A processing information acquisition system in a processing machine which feeds a processing point energy or material, the processing information acquisition system provided with a position information acquisition unit which acquires position information of a feed unit of energy or material, a feed rate control unit which receives a feed condition command of energy or material, converts the feed condition command to a control command which controls a feed of energy or material, and uses the converted control command to control a feed rate of energy or material from the feed unit, a feed rate estimation unit which acquires the control command from the feed rate control unit and calculates an estimated feed rate of energy or material which is fed to a processing point based on the control command, and an output unit which outputs the position information which the position information acquisition unit acquired and the estimated feed rate which the feed rate estimation unit calculated when the feed unit is located at a position corresponding to the position information. | 2012-02-09 |
20120035746 | AUTOMATIC RECEIVING, INSPECTION, INVENTORY MANAGEMENT AND REPORTING USING WIRELESS COMMUNICATIONS - A system for managing an inventory of process control devices in a process plant includes a computer workstation, a database storing instrument specification data for one or more process control devices used for controlling a process performed in the process plant environment, a wireless gateway adapted to wirelessly communicate with wireless enabled process control devices in the process plant environment, a communication bus interconnecting the wireless gateway, the computer workstation, and the database, an inventory control application executed by the computer workstation. The inventory control application is adapted to interrogate a received process control device via the wireless gateway to receive device data from the received process control device identifying and describing the received process control device. The inventory control application is further adapted to access the database to retrieve instrument specification data for the received process control device and compare the received device data to the retrieved instrument specification data. The inventory control application ensures that the received process control device corresponds to the instrument specification data. | 2012-02-09 |
20120035747 | SCALING AND PARAMETERIZING A CONTROLLER - Controller scaling and parameterization are described. Techniques that can be improved by employing the scaling and parameterization include, but are not limited to, controller design, tuning and optimization. The scaling and parameterization methods described here apply to transfer function based controllers, including PID controllers. The parameterization methods also applies to state feedback and state observer based controllers, as well as linear active disturbance rejection controllers. It is emphasized that this abstract is provided to comply with the rules requiring an abstract that will allow a searcher or other reader to quickly ascertain the subject matter of the application. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. 37 CFR 1.72(b). | 2012-02-09 |
20120035748 | INTERACTIVE SYSTEM FOR CONTROLLING MULTIPLE INPUT MULTIPLE OUTPUT CONTROL (MIMO) STRUCTURES - Exemplary embodiments allow users to interactively formulate and solve multivariable feedback control problems. For example, users can solve problems where a plurality of control elements are distributed over one or more feedback loops and need to be jointly tuned to optimize overall performance and robustness of a control system. Embodiments allow users to specify design requirements and objectives in formats familiar to the user. Embodiments can operate on tunable parameters to solve the control problem in a manner that satisfies the design requirements and/or objectives provided by the user. | 2012-02-09 |
20120035749 | SEAMLESS INTEGRATION OF PROCESS CONTROL DEVICES IN A PROCESS CONTROL ENVIRONMENT - In order to facilitate seamless integration of process control devices in a process control system, an integrated seamless diagnostic device collects diagnostic data related to the operation of (or problems associated with) one communication link that supports one process control protocol but communicates the collected diagnostic data to other entities in the process control system via another communication link that supports a different process control protocol. As a result, problems with the communication link monitored by the integrated seamless diagnostic device can be reported to the appropriate entities in the process control system as they occur and without unwanted delay. Moreover, problems with the monitored communication link can be communicated to the appropriate entities via process control protocols that are understood by those entities (and other entities in the process control system) and without consuming the potentially valuable resources of the monitored communication link. | 2012-02-09 |
20120035750 | Control System for Safely Operating at Least One Functional Component - A system includes a functional control unit and a controller. The functional control unit is configured to enable and disable operation of a functional component. The controller is configured to receive a sensor signal, evaluate safety quality of the sensor signal, generate an evaluation parameter representing the safety quality of the sensor signal, and output the sensor signal with the evaluation parameter as a pair for receipt by the functional control unit. The functional control unit is configured to control operation of the functional component depending on the safety quality indicated by the evaluation parameter. | 2012-02-09 |
20120035751 | METHODS AND A SYSTEM FOR DETECTING FRAUD IN BETTING AND LOTTERY GAMES - In one embodiment of the invention, a method to detect fraud includes a) receiving by the computer system from a source information regarding a plurality of played coupons for at least one game, wherein the plurality of played coupons comprises at least one first coupon; b) populating by the computer system a two-dimensional array for each played game from the received information, wherein the at least one two-dimensional array holds aggregated game statistics, c) storing by the computer system the at least one two-dimensional array with in a data structure; d) scanning, using the received information for the at least one first coupon, by the computer system the at least one data structure to identify at least one abnormal pattern; and e) generating, when the at least one abnormal pattern is identified, by the computer system an alert prior to a payout on the at least one first coupon. | 2012-02-09 |
20120035752 | DATA RECORDING DEVICE AND AUDIO SYSTEM - Technical Problem: It is an object of the present invention to provide a data recording device which records a data file in a recording unit at a high speed, and can also restore management data and a data file. | 2012-02-09 |
20120035753 | SEAMLESS SWITCHING BETWEEN RADIO AND LOCAL MEDIA - Systems and methods are provided for seamlessly switching media playback between a media broadcast, such as a radio broadcast, and media from a local media library. When an electronic device determines that an upcoming media item in a media broadcast is not of interest to a user, the electronic device can switch playback from the media stream to a media item from the electronic device local library. The selected local media item can be related to a previously broadcast media item to ensure continuity in the user's listening or viewing experience. The electronic device can switch away from the local media item and return to the media stream when the media stream again broadcasts media items or segments of interest to the user. | 2012-02-09 |
20120035754 | MANUFACTURING PROCESS AND APPARATUS HAVING AN INTERCHANGEABLE MACHINE TOOL HEAD WITH INTEGRATED CONTROL - A modular manufacturing system and methods of using are provided. The modular manufacturing system includes a plurality of manufacturing heads that perform different manufacturing processes. These heads may include multi-axial machining heads, fiber placement heads including fiber tow and fiber tape lay-up heads. The heads are fixably attachable to a single positioning system that can manipulate the various heads along a plurality of different degrees of freedom relative to a tool or material blank. | 2012-02-09 |
20120035755 | PROCESS CONTROL USING PROCESS DATA AND YIELD DATA - A method for monitoring a manufacturing tool features acquiring metrology data (“Step a”). Data is acquired for process variables for a first process step performed by the manufacturing tool (“Step b”). A mathematical model of the first process step based on the metrology data and the acquired data is created (“Step c”). Steps b and c are repeated for at least a second process step (“Step d”). An nth mathematical model is created based on the metrology data and the data for the process variables for each of the n process steps (“Step e”). A top level mathematical model is created based on the metrology data and the models created by steps c, d and e (“Step f”). A multivariate metric is calculated based on the top level model of step f and data from subsequent runs of the manufacturing tool. Service is performed if the metric satisfies a condition. | 2012-02-09 |
20120035756 | POST CURE TIRE SIPING FOR PREVENTING IRREGULAR WEAR - Tires in use wear in a host of ways. One negative manner in which tires, especially truck tires, may wear is in an irregular fashion. When this phenomenon happens, the tread of the tire may become unusable, forcing the user to replace the tire, which is undesirable. This patent application poses a new and useful way of preventing irregular wear involving the addition of a predetermined configuration of pipes, increasing the useful life of the tire tread. | 2012-02-09 |
20120035757 | IMPROVEMENT OF TIRE UNIFORMITY THROUGH IDENTIFICATION OF PROCESS SIGNATURES - A system and related method for improving tire uniformity includes providing a number (n) of test tires manufactured in a known order and identifying at least one candidate cyclic process effect with a corresponding frequency of introduction (f). A given uniformity parameter, such as radial or lateral run-out, balance, mass variation, radial lateral or tangential force variation, is measured for each tire in the test set, and measured data points are combined into a concatenated composite waveform. At least one process harmonic associated with each identified cyclic process effect is separated from the tire harmonics, for example, by Fourier transformation with identification of the process harmonics as positive integer multiples of the mth harmonic of the measured uniformity parameter where m=n/f. Once the process harmonics are extracted, filtered uniformity measurements can be provided or new tires can be built with the process effect minimized. | 2012-02-09 |