40th week of 2013 patent applcation highlights part 68 |
Patent application number | Title | Published |
20130261677 | GRAFT ANCHOR SYSTEM AND METHOD - A graft anchor has first and second arms each having a leading end, a trailing end, an inner surface, and an outer bone contactable surface. The graft anchor also has a resilient bridge extending between the inner surface of the first arm and the inner surface of the second arm to space apart the first arm and the second arm. The resilient bridge defines a graft receiving pathway between the inner surfaces of the first and second arms. The resilient bridge also defines a deflection point about which a force acting upon the resilient bridge in a direction from the leading end to the trailing end causes the leading ends of the first and second arms to move toward one another and the trailing ends of the first and second arms to move away from one another. | 2013-10-03 |
20130261678 | IMPLANTATION PIN, FIXATION DEVICE AND METHOD FOR IMPLANTING THE IMPLANTATION PIN - An implantation pin for implantation in a target structure has a pinhead and a shaft. The pinhead comprises a pinhead moulding portion comprising a moldable material which can be liquefied by application of mechanical energy such as ultrasonic vibration energy. A channel extends through the pinhead and the shaft, the channel connecting the pinhead molding portion to a discharge opening located at the shaft. The moldable material can be liquefied by applying mechanical energy in the form of ultrasonic vibrations via a fixation device including an ultrasonic sonotrode and a vibrating tip. The pressure applied by the vibrating tip can be transmitted via the border of the pinhead to the target structure while the liquefied mouldable material can be forced through the channel and the discharge opening into a gap between the implantation pin and a recess in a target structure thereby fixing the implantation pin in the target structure. | 2013-10-03 |
20130261679 | SPINAL IMPLANT SYSTEM AND METHOD - A system includes a sleeve including first and second arms each including an outer ramp and an inward projection, each of the arms defining a cavity. First and second extensions are configured for disposal in the cavities. A fastener includes walls defining an implant cavity and a distal portion. The walls each include first and second end surfaces and a locking cavity. The extensions are configured for translation relative to the sleeve between a first orientation such that the extensions engage the respective ramps to fix the projections with a respective locking cavity in a configuration to capture the fastener with the sleeve and a second orientation such that the extensions move out of engagement with the respective ramps so that the projections are movable out of engagement with the locking cavities to release the fastener from the sleeve. Methods of use are disclosed. | 2013-10-03 |
20130261680 | DEVICE FOR TENSIONING A FLEXIBLE BAND | 2013-10-03 |
20130261681 | SURGICAL IMPACT TOOL - A surgical impact tool comprises an electromagnetic impactor hermetically sealed within a sterilizable housing having one or more external mechanical coupling for transmitting an impact to an object external to the tool. The housing also contains an energy storage medium rechargeable through the hermetic seal, and electronic controls operable through the hermetic seal. | 2013-10-03 |
20130261682 | BONE GROWTH DEVICE AND METHOD - An intramedullary lengthening device includes a housing and a distraction shaft. The intramedullary lengthening device is placed within a cavity of two bone sections (either already separated or purposely separated for insertion of the device). The distraction shaft of the intramedullary lengthening device is attached to the one of the bone sections using, for example, one or more attachment screws. The housing of the intramedullary lengthening device is attached to the second bone section using, for instance, one or more attachment screws. Over the treatment period, the bone is continually distracted, creating a new separation into which osteogenesis can occur. In one embodiment, the intramedullary lengthening device includes an actuator and an extension rod, which can be attached to one other. | 2013-10-03 |
20130261683 | Method, Device and System for Targetted Cell Lysis - A method, device and system employs particles, such as nanoparticles, and an electric or electro-magnetic field, to cause cell death in target cells by non-thermal means. The method of causing targeted cell death comprises the steps of: introducing a particle to the interior of a target cell and exposing the target cell to a transient electromagnetic field for a sufficient time interval in order to cause cell death. The invention overcomes problems associated with similar methods as a result of the fact that a smaller electric field is applied because the particle enhances the effect of the electric field in its immediate vicinity, so reducing the field strength needed to achieve cell lysis and thereby reducing the risk of damage to healthy cells that may be in its vicinity. Apparatus for performing the method; as well as techniques of delivering particles and for producing particles are also described. | 2013-10-03 |
20130261684 | LEADS WITH X-RAY FLUORESCENT CAPSULES FOR ELECTRODE IDENTIFICATION AND METHODS OF MANUFACTURE AND USE - An implantable lead for an electrical stimulation system includes a lead body having a distal end, a proximal end, a longitudinal length, and a circumference; a plurality of electrodes disposed along the distal end of the lead body in an electrode array; a plurality of terminals disposed along the proximal end of the lead body; a plurality of conductors electrically coupling the plurality of electrodes to the plurality of terminals; and at least one capsule including an x-ray fluorescent material and disposed along the distal end of the lead body relative to the electrode array to indicate, when viewed fluoroscopically, an orientation of the electrode array. The plurality of electrodes includes a plurality of segmented electrodes. Each of the plurality of segmented electrodes extends partially around the circumference of the lead body. | 2013-10-03 |
20130261685 | COORDINATED HIS-BUNDLE PACING AND HIGH ENERGY THERAPY - A cardiac arrhythmia can be identified, such as a tachycardia or fibrillation episode (atrial or ventricular). In responses to the detected arrhythmia, a coordinated electrostimulation therapy can be provided using at least one of a defibrillation shock therapy, a pre-shock conditioning therapy, or a post-shock conditioning therapy. The pre-shock or post-shock conditioning therapies can include electrostimulation therapies provided to the natural electrical conduction system of the heart between the atrioventricular node and the Purkinje fibers, inclusive, such as at or near a His bundle of a heart. In an example, a defibrillation threshold can be reduced by providing a pre-shock conditioning electrostimulation therapy to the natural electrical conduction system of the heart between the atrioventricular node and the Purkinje fibers, inclusive, such as at or near a His bundle. | 2013-10-03 |
20130261686 | SHOCK TIMING TECHNOLOGY - A method for accurately determining timing points for T-wave shocks is particularly useful in a system for determining a cardiac shock strength in an implantable cardioverter defibrillator (ICD. The method involves acquiring at least one first signal, acquiring at least a second signal, comparing the signals, and selecting a timing point with the T-wave of the signal. The first and second signals may be two different aspects of a single electrogram, first and second electrograms, or a combination thereof. Comparison preferably involves signal alignment and qualitative analysis. | 2013-10-03 |
20130261687 | SYSTEMS AND METHODS FOR SELECTING PACING VECTORS BASED ON SITE OF LATEST ACTIVATION FOR USE WITH IMPLANTABLE CARDIAC RHYTHM MANAGEMENT DEVICES - Techniques are provided for use with an implantable cardiac stimulation device equipped with a multi-pole left ventricular (LV) lead and a right ventricular (RV) lead for identifying suitable pacing vectors. In one example, RV-LV delay times are measured while using different electrodes of the LV lead as cathodes for sensing. The LV electrode having the longest RV-LV delay time is identified and LV capture thresholds and diaphragmatic stimulation thresholds are measured for pacing vectors that employ that LV electrode as a cathode. Assuming at least one vector employing the selected LV electrode is found to have acceptable thresholds, the vector is selected for use in delivering pacing therapy with the selected LV electrode. If none of the pacing vectors employing the selected LV electrode has acceptable thresholds, another LV electrode is selected and the procedure is repeated. Examples with a multi-pole RV lead are also described. | 2013-10-03 |
20130261688 | DETERMINATION OF PHRENIC NERVE STIMULATION THRESHOLD - In an example of a method, the method includes testing for phrenic nerve stimulation (PS) threshold. If PS beats are detected at the pacing output level, analyzing the detected PS beats using criteria to determine if the pacing output level can be declared to be the PS threshold. If the pacing output level cannot be declared to be the PS threshold based on the analysis of the PS beat at the pacing output level, performing a PS beat confirmation procedure. The PS beat confirmation procedure may include delivering additional cardiac paces at the pacing output level to generate additional PS beats, and analyzing the detected PS beats using other criteria to determine if the pacing output level can be confirmed as the PS threshold. | 2013-10-03 |
20130261689 | METHODS, DEVICES AND SYSTEMS FOR CARDIAC RHYTHM MANAGEMENT USING AN ELECTRODE ARRANGEMENT - Various embodiments of the present invention are directed to systems, methods and devices for cardiac applications. One such device is directed to a catheter, and uses thereof, for capturing myocardium of a heart by delivering pacing signals to a location in the heart. The location is near a His Bundle of the heart. The catheter has a proximal end for interfacing with an electrical pacing signal source and a distal end. The distal end includes a fixation mechanism that attaches the catheter to heart tissue. First and second electrodes are also located at the distal end. Each electrode is individually addressable for providing pacing signals to the heart tissue and also arranged to physically contact the heart tissue when the fixation mechanism is attached to the heart tissue. | 2013-10-03 |
20130261690 | APPARATUS FOR TREATING THE PHYSIOLOGICAL ELECTRIC CONDUCTION OF THE HEART - A new pacemaker apparatus for treating the physiological electric conduction of the heart that includes a conduction abnormality in a ventricle. The pacemaker includes a pulse generator and a pacing electrode located in the heart, the pulse generator providing pacing signals to the pacing electrode. The pacemaker further includes a signal generation circuit that generates electrical signals from heart-related feedback signals that indicate that the pacing electrode is delivering the pacing signals in a region at or near the His bundle of the heart. The combination of the pulse generator and the signal generation circuit indicates that the pacing electrode is delivering the pacing signals in the region, at or near the His bundle of the heart, to electrically bypass the conduction abnormality of the heart in the ventricle. | 2013-10-03 |
20130261691 | SYSTEM AND METHOD FOR NEURAL STIMULATION - Various aspects provide an implantable device. In various embodiments, the device comprises at least one port, where each port is adapted to connect a lead with an electrode to the device. The device further includes a stimulation platform, including a sensing circuit connected to the at least one port to sense an intrinsic cardiac signal and a stimulation circuit connected to the at least one port via a stimulation channel to deliver a stimulation signal through the stimulation channel to the electrode. The stimulation circuit is adapted to deliver stimulation signals through the stimulation channel for both neural stimulation therapy and CRM therapy. The sensing and stimulation circuits are adapted to perform CRM functions. The device further includes a controller connected to the sensing circuit and the stimulation circuit to control the neural stimulation therapy and the CRM therapy. Other aspects and embodiments are provided herein. | 2013-10-03 |
20130261692 | NEUROMODULATION SYSTEM AND RELATED METHODS - Embodiments of the present invention describe a system and method of stimulating nerves during a medical procedure including positioning one or more electrodes in electrical contact with one or more nerves of a patient and electrically stimulating the one or more nerves during a lower urinary, rectal or medical procedure affecting the bowel sufficient to affect one or more of bladder activity, prostate function, incontinence, or pain. | 2013-10-03 |
20130261693 | SLEEP APNEA TREATMENT SYSTEM - Apparatus is provided for treating obstructive sleep apnea, including an external device ( | 2013-10-03 |
20130261694 | SYSTEMS AND METHODS FOR DELIVERING NEURAL THERAPY CORRELATED WITH PATIENT STATUS - Therapy systems for treating a patient are disclosed. Representative therapy systems include an implantable pulse generator, a signal delivery device electrically coupled to the pulse generator, and a remote control in electrical communication with the implantable pulse generator. The pulse generator can have a computer-readable medium containing instructions for performing a process that comprises collecting the patient status and stimulation parameter; analyzing the collected patient status and stimulation parameter; and establishing a preference baseline containing a preferred stimulation parameter corresponding to a particular patient status. | 2013-10-03 |
20130261695 | SELECTIVE HIGH FREQUENCY SPINAL CORD MODULATION FOR INHIBITING PAIN, INCLUDING CEPHALIC AND/OR TOTAL BODY PAIN WITH REDUCED SIDE EFFECTS, AND ASSOCIATED SYSTEMS AND METHODS - Selective high-frequency spinal chord modulation for inhibiting pain with reduced side affects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 50 KHz may be applied to the patient's spinal cord region from an epidural, cervical location to address at least one of high back pain, mid-back pain, low back pain, and leg pain without creating paresthesia in the patient. | 2013-10-03 |
20130261696 | SELECTIVE HIGH FREQUENCY SPINAL CORD MODULATION FOR INHIBITING PAIN, INCLUDING CEPHALIC AND/OR TOTAL BODY PAIN WITH REDUCED SIDE EFFECTS, AND ASSOCIATED SYSTEMS AND METHODS - Selective high-frequency spinal chord modulation for inhibiting pain with reduced side affects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 50 KHz may be applied to the patient's spinal cord region from an epidural, cervical location to address at least one of high back pain, mid-back pain, low back pain, and leg pain without creating paresthesia in the patient. | 2013-10-03 |
20130261697 | DEVICES FOR CONTROLLING SPINAL CORD MODULATION FOR INHIBITING PAIN, AND ASSOCIATED SYSTEMS AND METHODS, INCLUDING CONTROLLERS FOR AUTOMATED PARAMETER SELECTION - Devices for controlling spinal cord modulation for inhibiting pain, and associated systems and methods, including controllers for automated parameter selection are disclosed. A particular embodiment includes receiving a first input corresponding to a location of a signal delivery device implanted in a patient, establishing a positional relationship between the signal delivery device and an anatomical feature of the patient, receiving a second input corresponding to a medical indication of the patient, and, based at least in part on the positional relationship and the indication, automatically identifying a signal delivery parameter in accordance with which a pulsed electrical signal is delivered to the patient via the signal delivery device. | 2013-10-03 |
20130261698 | THERAPY CONTROL USING RELATIVE MOTION BETWEEN SENSORS - The invention is directed to controlling therapy delivery based on a relative motion between a first and second activity sensor. The relative motion between the activity sensors is representative of the relative motion between the locations of the body of the patient at which the respective activity sensors are located. The use of relative motion, however, may substantially remove motion experienced by both the activity sensors, e.g., motion caused by the environment in which patient is located, thus providing a new reference frame from which to analyze the motion measurements. The relative motion may be used to detect a condition of a movement disorder and/or control delivery of the therapy delivered to patient to treat or reduce the condition. | 2013-10-03 |
20130261699 | METHOD AND APPARATUS FOR THE TREATMENT OF FOCAL DYSTONIA - A method and apparatus for using low levels of electrical stimulation to treat focal dystonia by stimulating the afferent nervous system and/or altering the function of the gamma motor neurons innervating muscles which experience symptomatic spasms. | 2013-10-03 |
20130261700 | EYE IMPLANT APPARATUS AND UPDATE SYSTEM FOR THE SAME - The present disclosure discloses an apparatus to be implanted in eyes, including: a configuration memory used for storing signal parameter configuration; a signal generator connected to the configuration memory and used for generating stimulating signals according to the signal parameter configuration in the configuration memory; electrodes connected to the signal generator and contact with outer surface of eye ball after implanted; a communication assembly connected to the configuration memory and used for receiving the signal parameter configuration, storing the received signal parameter configuration in the configuration memory; and a power supply connected to the configuration memory, signal generator and communication assembly, used for providing power. An update system for the apparatus is also disclosed. By using the above apparatus and update system, when it needs to change waveform parameter of stimulating signals, there is no need to take the apparatus out, reducing harm on human body and improving safety. | 2013-10-03 |
20130261701 | IMPLANTABLE ACTUATOR FOR HEARING STIMULATIOIN - There is provided an implantable actuator for stimulating a patient's hearing, comprising a support frame ( | 2013-10-03 |
20130261702 | UTERINE ELECTRICAL STIMULATION SYSTEM AND METHOD - Systems and methods for applying stimulating current to a patient for treating insufficient uterine contractions are provided. The system includes stimulation electrodes of a balloon electrode array device, a ring electrode array device, an electrode probe device, or a mesh electrode array device. Some aspects of the invention also provide a connector and cable device for coupling the stimulation electrodes to electronics for generating and providing the stimulating current to the stimulation electrodes. | 2013-10-03 |
20130261703 | POWERING MULTIPLE IMPLANTABLE MEDICAL THERAPY DELIVERY DEVICES USING FAR FIELD RADIATIVE POWERING AT MULTIPLE FREQUENCIES - A system includes a first implantable medical device configured to receive a first far field radiative signal at a first frequency from an external transmitter to charge a first charge storage device. The first implantable medical device includes a first therapy delivery unit powered by the first charge storage device. The first therapy delivery unit delivers a first therapy to a first target tissue of a patient. The system also includes a second implantable medical device configured to receive a second far field radiative signal at a second frequency from the external transmitter to charge a second charge storage device. The second implantable medical device includes a second therapy delivery unit powered by the second charge storage device. The second therapy delivery unit delivers a second therapy to a second target tissue of the patient. | 2013-10-03 |
20130261704 | External Charger for a Medical Implantable Device Using Field Sensing Coils to Improve Coupling - By incorporating magnetic field sensing coils in an external charger, it is possible to determine the position of an implantable device by sensing the reflected magnetic field from the implant. In one embodiment, two or more field sensing coils are arranged to sense the reflected magnetic field. By comparing the relative reflected magnetic field strengths of the sensing coils, the position of the implant relative to the external charger can be determined. Audio and/or visual feedback can then be communicated to the patient to allow the patient to improve the alignment of the charger. | 2013-10-03 |
20130261705 | METHOD AND APPARATUS FOR THE TREATMENT OF SPASMODIC DYSPHONIA - A method and apparatus for using low levels of electrical stimulation to treat spasmodic dysphonia by stimulating the afferent nervous system and/or altering the function of gamma motor neurons innervating muscles which experience symptomatic spasms. | 2013-10-03 |
20130261706 | SYSTEMS AND METHODS FOR APPLYING RAPID SEQUENTIAL ELECTRODE STIMULATION - Described herein are methods and systems for delivering a burst of stimulation pulses or pulse segments sequentially to a plurality of stimulation pathways. The stimulation pulses may be generated by a stimulation device, which may comprise an implantable neurostimulator. The stimulation pathways may comprise one or more electrodes electrically connected to the stimulation device. In some variations, the stimulation pathway may comprise a monopolar stimulation pathway and/or a bipolar stimulation pathway. | 2013-10-03 |
20130261707 | PHOTORECEPTOR SYSTEM FOR MELATONIN REGULATION AND PHOTOTHERAPY - The present invention involves a light system for stimulating or regulating neuroendocrine, circadian, and photoneural systems in mammals based upon the discovery of peak sensitivity ranging from 425-505 nm; a light meter system for quantifying light which stimulates or regulates mammalian circadian, photoneural, and neuroendocrine systems. The present invention also relates to translucent and transparent materials, and lamps or other light sources with or without filters capable of stimulating or regulating neuroendocrine, circadian, and photoneural systems in mammals. Additionally, the present invention involves treatment of mammals with a wide variety of disorders or deficits, including light responsive disorders, eating disorders, menstrual cycle disorders, non-specific alerting and performance deficits, hormone-sensitive cancers, and cardiovascular disorders. | 2013-10-03 |
20130261708 | SUBSTITUTED TETRAARYLBENZENES - The present invention relates to substances, to electroluminescent device comprising these substances, and to the use thereof. | 2013-10-03 |
20130261709 | WARMING THERAPY DEVICE - A heat therapy device including a care unit presenting a lying surface for supporting an infant, a hood ( | 2013-10-03 |
20130261710 | BLOCK COPOLYMER (BCP) ENCAPSULATED NANOPARTICLES AND METHODS OF USE THEREOF - This invention provides block copolymer (BCP) encapsulated nanoparticles. The BCP-encapsulated nanoparticles are used in methods for targeting a tumor, in methods of imaging a tumor and in methods of treating cancer including hyperthermia of tumors. This invention further provides processes for preparation of BCP-encapsulated nanoparticles. | 2013-10-03 |
20130261711 | METHODS TO ARREST CANCER CELL GROWTH AND PROLIFERATION USING ELECTROMAGNETIC ENERGY DELIVERED VIA ELECTROMAGNETIC COIL SYSTEMS - A non-invasive method of using electromagnetic field energies to reduce or arrest the growth rate and proliferation of cancer cells, and induce apoptosis in cancer cells, and reduce or arrest the growth and survival of foreign pathogens, relatively without significantly harming normal cells beyond their physiologic threshold of survival are provided. The methods described herein are intended to be used toward the treatment of cancer in human or animals within the context of cancer therapeutics. | 2013-10-03 |
20130261712 | COLD THERAPY DEVICE - The present invention is directed to a device for absorbing heat from a body. More particularly, the invention pertains to an improved device which utilizes a gel material comprising liquids and solids to absorb, over an extended period of time, heat from a body. The present invention also includes methods of providing cold therapy treatment to a user | 2013-10-03 |
20130261713 | EMBOLIC COIL DETACHMENT MECHANISM WITH FLEXIBLE DISTAL MEMBER AND RESISTIVE ELECTRICAL HEATING ELEMENT - An embolic coil detachment system includes an elongated, flexible polymer tube having a tubular wall with an inner surface defining an interior lumen. A distal portion of the tubular wall has a score line, and a resistive heating element is located near the score line and in immediate contact with a surface of a distal portion of the tubular wall, to provide direct heating of the distal portion of the flexible polymer tube adjacent to the score line. A therapeutic embolic coil includes a headpiece that is releasably attached within the distal portion of the flexible polymer tube, and that is releasable by heating of the distal portion of the tubular shaft to cause the distal portion of the tubular wall to split along the score line. | 2013-10-03 |
20130261714 | STEROID ELUTING COLLAR UNDERMOLD - Methods of manufacturing implantable medical devices with one or more undermolded features are disclosed. An example method includes injection molding an annular-shaped member onto an inner surface of a sacrificial mold insert, and then undermolding an elongate medical device body directly to the member. The member is directly coupled to the device body without the use of adhesives or bonding agents, thus eliminating the presence of gaps or surface irregularities that can affect device performance. | 2013-10-03 |
20130261715 | MEDICAL LEADS - Medical leads, such as medical electrical leads and medical neurological leads, that include a polymeric material that includes a silicone-urethane-containing polymer having improved hydrolytic stability. | 2013-10-03 |
20130261716 | SUBCUTANEOUS IMPLANTABLE CARDIOVERTER-DEFIBRILLATOR PLACEMENT METHODS - A subcutaneous cardiac device includes two electrodes and a stimulator that generates a pulse to the electrodes. The electrodes are implanted between the skin and the rib cage of the patient and are adapted to generate an electric field corresponding to the pulse, the electric field having a substantially uniform voltage gradient as it passes through the heart. The shapes, sizes, positions and structures of the electrodes are selected to optimize the voltage gradient of the electric field, and to minimize the energy dissipated by the electric field outside the heart. More specifically, the electrodes have contact surfaces that contact the patient tissues, said contact surfaces having a total contact area of less than 100 cm | 2013-10-03 |
20130261717 | Retinal Prosthesis and Method of Manufacturing a Retinal Prosthesis - The present invention is an improved package and configuration for an implantable retinal prosthesis. The retinal prosthesis of the present invention includes an electrode array suitable to be mounted in close proximity to a retina, an electronics package and inductive receiving coil mounted next to each other on a strap surrounding the sclera so that the height above the sclera of the prosthesis is minimized. | 2013-10-03 |
20130261718 | METHOD AND APPARATUS FOR DETERMINING RELATIVE POSITIONING BETWEEN NEUROSTIMULATION LEADS - A method and neurostimulation control system for operating two leads disposed adjacent tissue of a patient are provided. A plurality of cross-lead electrical parameters are measured to generate a measured electrical profile of the electrode leads. A plurality of cross-lead electrical parameters are estimated to generate a first reference electrical profile for the electrode leads in a first known staggered configuration. The first reference electrical profile is spatially shifted to generate a second reference electrical profile for the electrode leads in a second known staggered configuration. The measured electrical profile is compared to the first and second reference electrical profiles, and a longitudinal stagger between the electrode leads is quantified based on the comparison. | 2013-10-03 |
20130261719 | ANCHOR FOR IMPLANTABLE MEDICAL DEVICE - In some examples, an anchor for a therapy delivery element includes a body portion including a lumen extending though the body portion. The body portion includes a first configuration in which the lumen is linear, the body portion in the first configuration being configured to receive the therapy delivery element within the lumen. The body portion also includes a second configuration in which the lumen is non-linear, wherein the lumen of the body portion in the second configuration frictionally engages the therapy delivery element. | 2013-10-03 |
20130261720 | Housing-Interface Assembly To Be Implanted In A Bone Wall For Enabling An Interaction Between A Human Activity And A Machine - An extraoral bone-anchored implant device includes an anchoring component ( | 2013-10-03 |
20130261721 | ELECTRODE CUFFS - An electrode assembly includes electrodes and a cuff, shaped so as to define a tubular housing that defines a longitudinal axis therealong, two edges, and a slit between the two edges. When the housing is closed, respective contact surfaces of the two edges touch each other, and the housing defines an inner surface that faces and surrounds the axis, to which inner surface the electrodes are fixed. The cuff further defines three or more annular insulating elements that extend toward the axis from the inner surface of the housing at respective longitudinal positions along the housing, such that the inner surface of the housing and pairs of the insulating elements define, at respective longitudinal positions along the housing, respective chambers open toward the axis. The housing is shaped such that the contact surfaces of the two edges extend toward the axis and protrude into the chambers. | 2013-10-03 |
20130261722 | Treatment Of Diabetic Patients With Stent And Locally Administered Adjunctive Therapy - Embodiments of the present invention include methods of treating, preventing, and/or ameliorating a vascular disease and/or disorder in a diabetic or pre-diabetic patient. The methods include implanting a stent in a vascular region in a diabetic or pre-diabetic patient, and prior to and/or during the implantation procedure, delivering a lubricant formulation to the vascular region. The stent may be a bare metal stent, or a drug eluting stent, such as a metal stent with a coating including a drug, such as everolimus or sirolimus. | 2013-10-03 |
20130261723 | Treatment Of Diabetic Patients With A Drug Eluting Stent And A Drug Coated Balloon - Embodiments of the present invention include methods for the treatment, prevention, or amelioration of vascular disease and/or disorder in diabetic patients. The methods include implantation of a stent including a drug, and the use of a drug coated balloon. The DES may be a DES having a metal body and a coating including the drug, or a bioabsorbable stent with drug in the body of the stent, in a coating on the stent, or both in the body of the stent and in a coating on the stent. | 2013-10-03 |
20130261724 | DEVICES AND METHODS FOR TREATMENT OF VASCULAR ANEURYSMS - The present invention relates to devices and methods for the treatment of diseases in the vasculature, and more specifically, devices and methods for treatment of aneurysms found in blood vessels. In a first embodiment of the present invention, a two part prostheses, where one part is an expandable sponge structure and the other part is an expandable tubular mesh structure, is provided. In the first embodiment, the expandable sponge structure is intended to fill the aneurysm cavity to prevent further dilatation of the vessel wall by creating a buffer or barrier between the pressurized pulsating blood flow and the thinning vessel wall. In the first embodiment, the expandable tubular mesh structure is placed across the aneurysm, contacting the inner wall of healthy vessel proximal and distal to the aneurysm. | 2013-10-03 |
20130261725 | STENT HOLDING STRUCTURE FOR INTRODUCERS - An implantable medical device includes a carrier element having a distal holding member ( | 2013-10-03 |
20130261726 | FORCED DEPLOYMENT SEQUENCE - A fixed sequence activation handle is described that forces a predetermined activation sequence. Such handles are suitable for use in the delivery of medical devices or for other application that require a fixed sequence of activations. | 2013-10-03 |
20130261727 | VARIABLE ZONE HIGH METAL TO VESSEL RATIO STENT AND METHOD - A variable zone high metal to vessel ratio stent includes a proximal high metal to vessel ratio zone, a central low metal to vessel ratio zone, and a distal high metal to vessel ratio zone. The proximal high metal to vessel ratio zone is deployed with fixation and sealing to healthy tissue of a main vessel superior to branch vessels and an aneurysm. The central low metal to vessel ratio zone is deployed directly on ostai of the branch vessels. However, as the central low metal to vessel ratio zone is highly permeable, blood flows from the main vessel through the central low metal to vessel ratio zone and into branch vessels. | 2013-10-03 |
20130261728 | HIGH METAL TO VESSEL RATIO STENT AND METHOD - A method includes covering ostai of branch vessels emanating from a main vessel and an aneurysm with a high metal to vessel ratio stent. A metal to vessel ratio of the high metal to vessel ratio stent is sufficiently high to encourage tissue ingrowth around the high metal to vessel ratio stent yet is sufficiently low to ensure perfusion of the branch vessels through the high metal to vessel ratio stent. The ingrowth of tissue provides secure fixation and sealing of the high metal to vessel ratio stent to the main vessel and remodels and essentially eliminates the aneurysm. Further, as the entire high metal to vessel ratio stent is permeably, the high metal to vessel ratio stent is deployed without having to rotationally position the high metal to vessel ratio stent. | 2013-10-03 |
20130261729 | CONTROL OF BALLOON INFLATION RATE DURING DEPLOYMENT OF SCAFFOLD - An apparatus and method for controlling inflation pressure and pressurization rate of a balloon during deployment of a stent or scaffold is disclosed. | 2013-10-03 |
20130261730 | ANEURYSM OCCLUSION SYSTEM AND METHOD - An aneurysm occlusion system includes a device positionable within a cerebral blood vessel covering a neck of an aneurysm on the blood vessel. The device includes an expandable tubular element having a lumen surrounded by a sidewall including a plurality of gaps. When expanded, the tubular element includes longitudinal standards arrayed helically in a proximal to distal direction. The standards support struts and the gaps are defined between adjacent struts and are sufficiently large to permit delivery of embolic coils or other embolic materials therethrough. | 2013-10-03 |
20130261731 | Curved Stent Graft Assembly - A stent graft assembly comprises a graft of flexible material supported by a stent frame that is configured to be deformable between an expanded state and a radially collapsed state. The graft of flexible material has the shape of a tube that is curved along a longitudinal axis of the tube when the graft is in an expanded, undeformed state. The stent graft assembly is deformable into a state in which the graft is deformed into the shape of a tube that is straight. The stent graft assembly may be designed for treatment of a thoracic aorta aneurysm. | 2013-10-03 |
20130261732 | INTEGRATED MESH HIGH METAL TO VESSEL RATIO STENT AND METHOD - A method includes covering ostai of branch vessels emanating from a main vessel and an aneurysm with an integrated mesh high metal to vessel ratio stent. The integrated mesh high metal to vessel ratio stent includes serpentine rings integrated with an integrated mesh having holes formed therein. A metal to vessel ratio of the integrated mesh high metal to vessel ratio stent is sufficiently high to encourage tissue ingrowth around the integrated mesh high metal to vessel ratio stent yet is sufficiently low to ensure perfusion of the branch vessels through the integrated mesh high metal to vessel ratio stent. | 2013-10-03 |
20130261733 | Coil Bioabsorbable Stents - An expandable, bioabsorbable stent having a coiled-coil configuration is described. The stent further comprises regions of variable pitch that allow for variation in either rigidity, or variability diameter within sub-regions along the length of the deployed stent. By varying the diameter allows the stent to extend into regions such as branched vessels, or into the neck of aneurysms. In some embodiments, the stent comprises longitudinal support fibers that run substantially the length of the deployed stent to provide additional strength. In addition, the stent may also comprise regional support fibers that run less than the length of the stent, and which provide increased regional strength while permitting flexibility of the stent. The stent further comprises micro-tubes that are configured to be visible using medical imaging techniques. The stent can be manufactured from materials that are bioabsorbable and/or include the ability to release pharmacologically active substances over time. | 2013-10-03 |
20130261734 | ADVANCED KINK RESISTANT STENT GRAFT - Stent-grafts for treating thoracic aortic aneurysms and abdominal aortic aneurysms include graft portions having inflatable channels and graft extensions. The graft extensions include an undulating wire stent and porous, but substantially fluid impermeable, polytetrafluoroethylene (PTFE) graft materials. | 2013-10-03 |
20130261735 | MAGNESIUM ALLOY IMPLANTS WITH CONTROLLED DEGRADATION - Stents or scaffolds made from magnesium or magnesium alloys including additives or barrier coatings that modify the corrosion rate of the stent are disclosed. Methods of forming barrier coatings that modify the corrosion rate of the stent are disclosed. | 2013-10-03 |
20130261736 | MULTILAYER BIOABSORBABLE SCAFFOLDS AND METHODS OF FABRICATING - A bioabsorbable scaffold composed of a multilayer structure of alternating layers of different polymers is disclosed. The multilayer structure can have 20 to 1000 layers and the individual thickness of the layers can be 0.2 to 5 microns. A method of making the scaffold including a layer multiplying extrusion process is disclosed. | 2013-10-03 |
20130261737 | Dual Valve Prosthesis for Transcatheter Valve Implantation - A dual valve prosthesis having first and second prosthetic valve sections is disclosed. The first prosthetic valve section includes a stent structure with a first prosthetic valve secured therein and the second prosthetic valve section includes an annular frame with a second prosthetic valve secured therein. When the dual valve prosthesis is in an expanded configuration, the annular frame extends from the stent structure such that the first and second prosthetic valves are laterally offset from each other. In a method in accordance herewith, the first and second prosthetic valve sections include prosthetic aortic and mitral valves, respectively, and the dual heart valve prosthesis is configured to replace both the native aortic and mitral valves of the heart in a single transcatheter heart valve implantation procedure. | 2013-10-03 |
20130261738 | Dual Valve Prosthesis for Transcatheter Valve Implantation - A dual valve prosthesis having first and second prosthetic valve components with a linkage that connects the first and second prosthetic valve components together is disclosed. Each of the first and second prosthetic valve components includes a stent structure with a prosthetic valve secured therein. In a disclosed method, the first and second prosthetic valve components include prosthetic mitral and aortic valves, respectively, and the dual heart valve prosthesis is configured to replace both the native mitral and aortic valves of the heart in a single transcatheter heart valve implantation procedure. The linkage between the first and second prosthetic valve components is configured to secure the anterior mitral valve leaflet against a wall of the left ventricle when the dual valve prosthesis is implanted within the heart. | 2013-10-03 |
20130261739 | Dual Valve Prosthesis for Transcatheter Valve Implantation - A dual valve prosthesis having a self-expanding anchoring frame with first and second prosthetic valve assemblies attached to the anchoring frame is disclosed. Each of the first and second prosthetic valve assemblies includes a balloon-expandable stent structure with a prosthetic valve secured therein. In a disclosed method, the first and second prosthetic valve assemblies include prosthetic mitral and aortic valves, respectively, and the dual heart valve prosthesis is configured to replace both the native mitral and aortic valves of the heart in a single transcatheter heart valve implantation procedure. | 2013-10-03 |
20130261740 | Valve Prosthesis - Heart valve prostheses are provided having a self-expanding frame that supports a valve body comprising a skirt and a plurality of coapting leaflets. The leaflets are constructed with four commissure points to reduce the stress and strain applied to the commissure points and to efficiently distribute and transmit forces along the leaflets and to the frame. | 2013-10-03 |
20130261741 | Prosthetic Heart Valves and Devices, Systems and Methods for Prosthetic Heart Valves - Described herein is a unique sutureless heart valve that includes a deployment mechanism having a plurality of fasteners. The plurality of fasteners may be actuated at least two states: a disengaged state wherein said plurality of fasteners are retracted, and an engaged state wherein said plurality of fasteners are extended; and further comprising a deployed state wherein said plurality of fasteners, when extended, are irreversibly locked such that said heart valve is securely deployed at the target surgical site. The valve deployment mechanism comprises a ring assembly comprising a first annular member onto which said plurality of fasteners are associated and a second annular member peripheral to said first annular member and comprising a series of windows through which individual fasteners of said plurality of fasteners project. | 2013-10-03 |
20130261742 | KIT FOR THE MANIPULATION OF IMPLANTABLE MEDICAL DEVICES - A kit for facilitating crimping of a prosthetic heart valve for implantation at an aortic valve site in a human heart, the aortic valve site including a plurality of valve sinuses, the kit comprising a prosthetic aortic heart valve having a tubular structure and a first central axis including an anchoring structure comprising an annular outflow member, an annular inflow member, and a plurality of axial connection formations arranged in pairs angularly distributed around the central axis, and a plurality of leaflets coupled to the anchoring structure and adapted to substantially allow blood flow in a first direction and to substantially prevent blood flow in a second direction. The kit further includes a holder member comprising a first disc support member that includes a central hub and a plurality of bridge elements, wherein the hub and the bridge elements extend axially from opposite sides of the disc support member; and a second ring support member that includes receptacles for coupling with the bridge elements, and a plurality of finger formations protruding axially from the ring member and extending lengthwise along at least a portion of the prosthetic aortic heart valve. | 2013-10-03 |
20130261743 | SYSTEM CONTROLLER FOR VARIABLE-OPTIC ELECTRONIC OPHTHALMIC LENS - A system controller for an ophthalmic lens comprising an electronic system which actuates a variable-focus optic is disclosed herein. The system controller is part of an electronic system incorporated into the ophthalmic lens. The electronic system includes one or more batteries or other power sources, power management circuitry, one or more sensors, clock generation circuitry, control algorithms and circuitry, and lens driver circuitry. The controller including multiple state machines configured as digital logic gates. | 2013-10-03 |
20130261744 | IMPLANTABLE OPHTHALMIC DEVICE WITH AN ASPHERIC LENS - Implantable ophthalmic devices with aspheric lenses and dynamic electro-active elements offer excellent depth of field and image quality while providing high optical throughput. An exemplary implantable ophthalmic device includes an aspheric lens with a negative spherical aberration that varies with radius. The aspheric lens can have peak optical powers at its geometric centers surrounded by a region of varying optical power (with varying slope) that extends radially from its center. When implanted, these aspheric lenses provide an incremental optical power that varies as a function of pupil diameter, which changes with object distance, for viewing far, intermediate, and near objects. The aspheric lens may also bonded or integrally formed with a spherical lens that provides fixed optical power for viewing far objects and/or a dynamic electro-active element that with two or more states (e.g., on and off) for increasing the effective optical power when viewing near objects. | 2013-10-03 |
20130261745 | DUAL PLANE BREAST IMPLANT - A soft breast prosthesis is provided, the prosthesis having a surface configuration advantageous for dual plane placement of the prosthesis in a breast. | 2013-10-03 |
20130261746 | IMPLANTABLE INTER-VERTEBRAL DISK HAVING UPPER AND LOWER LAYERS OF A METAL EXHIBITING BONE FUSING CHARACTERISTICS AND WHICH SANDWICH THEREBETWEEN A SOFT PLASTIC CUSHIONING DISC FOR PROVIDING DYNAMIC PROPERTIES MIMICKING THAT OF A NATURAL INTER-VERTEBRAL DISC - The present invention discloses an inter-vertebral and implantable disk substituting for a fibro cartilage and including first and second hard outer layers between which is sandwiched a softer inner cushioning layer. Each of the outer layers includes an exterior texturized pattern for promoting bone in-growth subsequent to implantation. Each of the outer layers may also include an exteriorly integrally formed and angled mounting portion including an interiorly positioned aperture. The mounting portions are adapted to being applied against reconditioned side exterior locations of first and second succeeding intervertebral bodies and mounted to the bodies with a screw or clip. | 2013-10-03 |
20130261747 | ALIF Spinal Implant - Spinal fusion appliances, delivery devices and methods of using the same are provided. In various embodiments, the appliances include a housing and a flexible tape with opposite ends that are optionally adjustable using an actuator within the housing. | 2013-10-03 |
20130261748 | Hydraulically Actuated Expanding Spine Cage with Extendable Locking Anchor - A spinal implant which is configured to be deployed between adjacent vertebral bodies. The implant has at least one extendable support element with a retracted configuration to facilitate deployment of the implant and an extended configuration so as to expand the implant and effectively distract the disc space, stabilize the motion segments and eliminate pathologic spine motion. Angular deformities can also be corrected, and natural curvatures restored. Preferably, the implant has a minimal dimension in its unexpanded state that is smaller than the dimensions of the neuroforamen through which it typically passes to be deployed within the intervertebral space. The implant is provided with a locking system preferably having a plurality of locking elements to lock the implant in an extended configuration. Bone engaging anchors also may be provided to ensure secure positioning | 2013-10-03 |
20130261749 | Advanced Intra-spinal Decompression Implant - A new intra-spinal decompression implant is introduced. One example for our presentation is a device with 2 or 3 pieces, with each piece with 2 clamps, symmetrically located on each side of each piece. The main piece has at least 2 screws which engage into 2 or more grooves in the side piece, to get attached to the side piece. The 3 | 2013-10-03 |
20130261750 | REVERSE SHOULDER ORTHOPAEDIC IMPLANT HAVING A METAGLENE COMPONENT WITH A SCREW LOCKING CAP - A reverse shoulder orthopaedic implant includes a glenosphere component having a lateral bearing surface configured to articulate with a humeral cup of a humeral prosthesis. A metaglene component includes a platform configured to receive glenosphere component. | 2013-10-03 |
20130261751 | REVERSE SHOULDER ORTHOPAEDIC IMPLANT HAVING AN ELLIPTICAL GLENOSPHERE COMPONENT - A reverse shoulder orthopaedic implant includes a glenosphere component having a lateral bearing surface configured to articulate with a humeral cup of a humeral prosthesis. A metaglene component includes a platform configured to receive glenosphere component. | 2013-10-03 |
20130261752 | GLENOID DEFECT-FILLING COMPONENT - An orthopaedic shoulder prosthesis includes glenoid defect-filling component configured to be implanted within a defect in a glenoid of a patient. The glenoid defect-filling component includes a porous metallic body and a plurality of holes formed in the porous metallic body, the plurality of holes being arranged in a pattern to receive a number of pegs of a discrete polymer glenoid component. | 2013-10-03 |
20130261753 | METHOD OF IMPLANTING A GLENOID DEFECT-FILLING COMPONENT - An orthopaedic shoulder prosthesis includes glenoid defect-filling component configured to be implanted within a defect in a glenoid of a patient. The glenoid defect-filling component includes a porous metallic body and a plurality of holes formed in the porous metallic body, the plurality of holes being arranged in a pattern to receive a number of pegs of a discrete polymer glenoid component. | 2013-10-03 |
20130261754 | STEMLESS HUMERAL COMPONENT OF AN ORTHOPAEDIC SHOULDER PROSTHESIS - A stemless humeral component for replacing the humeral head of a patient's humerus includes a support flange having a number of cantilevered legs extending distally away from a bottom surface thereof. Instruments and methods for surgically installing the stemless humeral component are also disclosed. | 2013-10-03 |
20130261755 | SURGICAL METHOD FOR IMPLANTING A STEMLESS HUMERAL COMPONENT TO THE HUMERUS OF A PATIENT - A stemless humeral component for replacing the humeral head of a patient's humerus includes a support flange having a number of cantilevered legs extending distally away from a bottom surface thereof. Instruments and methods for surgically installing the stemless humeral component are also disclosed. | 2013-10-03 |
20130261756 | KNEE IMPLANTS HAVING HYDROMAGNETIC JOINTS - A knee implant includes a first implant part adapted for attachment to a femur and a second implant part adapted for attachment to a tibia. The knee implant includes a hydromagnetic joint having a first magnetic element with a first magnetically charged surface and a first buoyant element coupled with the first magnetic element, and a second magnetically charged surface that opposes the first magnetically charged surface of the first magnetic element and a second buoyant element coupled with the second magnetic element. A fluid body is disposed between the first and second buoyant elements, and the first and second buoyant elements are in fluid communication with one another through the fluid body. The hydromagnetic joint has an enclosure extending between the first and second buoyant elements for containing the fluid body therebetween, whereby the first and second buoyant elements are moveable relative to one another. | 2013-10-03 |
20130261757 | TIBIAL PROSTHESIS SYSTEMS, KITS, AND METHODS - Tibial prosthesis systems for implantation or use in a knee joint are disclosed. A tibial prosthesis system can include a bearing component, a base component, a shim component, and optionally a spacer component. The shim or spacer component can be inserted between an inferior surface of the bearing component and a superior surface of the base component. The insertion of the shim or spacer component can provide spacing adjustment between the bearing and base components. The shim component can include one or both of a medial edge having a different height than a lateral edge or an anterior edge having a different height than a posterior edge. The differing edge height of the shim component can provide a surgeon with knee joint kinematic insight regarding an angled bone cut before the cut is made, and can allow for sizing of an appropriately permanent prosthesis system using a reduced number of provisional components. | 2013-10-03 |
20130261758 | TIBIAL PROSTHESIS SYSTEMS, KITS, AND METHODS - Tibial prosthesis methods for balancing a knee joint during a surgical procedure are disclosed. A method can comprise inserting a first tibial shim component between a tibial bearing component and a tibial base or a tibial plate component in an anterior/posterior direction. The first tibial shim component can include one or both of a medial edge having a different height than a lateral edge or an anterior edge having a different height than a posterior edge. The method can further comprise testing one or more of a stability, a force balance, or a range of motion of a knee joint in which the first tibial shim component is inserted. If the testing result is not satisfactory, the method can include removing the first tibial shim component, and inserting a second tibial shim component between the tibial bearing component and the tibial base or tibial plate component in the anterior/posterior direction. | 2013-10-03 |
20130261759 | TIBIAL PROSTHESIS SYSTEMS, KITS, AND METHODS - Tibial prosthesis systems for implantation or use in a knee joint are disclosed. A tibial prosthesis system can include a bearing component, a base component, a shim component, and optionally a spacer component. The shim or spacer component can be inserted between an inferior surface of the bearing component and a superior surface of the base component. The insertion of the shim or spacer component can provide spacing adjustment between the bearing and base components. The shim component can include one or both of a medial edge having a different height than a lateral edge or an anterior edge having a different height than a posterior edge. The differing edge height of the shim component can provide a surgeon with knee joint kinematic insight regarding an angled bone cut before the cut is made, and can allow for sizing of an appropriately permanent prosthesis system using a reduced number of provisional components. | 2013-10-03 |
20130261760 | METHOD FOR PLANNING POSITIONING OF A BALL JOINT PROSTHESIS - The present invention relates to a method for planning the positioning of a ball joint prosthesis, in particular a hip joint prosthesis, wherein the prosthesis includes a stem and a cup and the method comprises the following steps: —determining the position of at least one point lying on the rim of the joint socket, in particular the position of at least two points lying in an anterior region of the acetabulum; —defining a requirement for the position and/or orientation of the cup on the basis of the determined positions of the at least one point. The present invention also relates to a method for optimising the positioning of a ball joint prosthesis, in particular a hip joint prosthesis, wherein the prosthesis includes a stem and a cup and the method comprises the following steps: —defining at least one requirement for the position and/or orientation of the cup; —calculating an optimum position and/or orientation of the cup on the basis of all the defined requirements being fulfilled. | 2013-10-03 |
20130261761 | MOBILE BEARING HIP ASSEMBLY HAVING DECOUPLED MOTION ALONG MULTIPLE AXES - An acetabular hip implant includes an acetabular shell component, a first insert secured to the acetabular shell component, a second insert secured to the first insert, and a femoral head configured to be secured to the second insert. The first insert is permitted to rotate relative to the acetabular shell about a first axis, the second insert is permitted to rotate relative to the first insert about a second axis, and the femoral head is permitted to rotate relative to the second insert about a third axis. | 2013-10-03 |
20130261762 | Hip surgery neck and ball adjustment apparatus and method - The method of accurately and correctly fitting and axially positioning at implantable ball to the neck trunnion of a hip replacement device, as during surgery, the ball adapted to be received in a socket, the ball having a bore, the method including the step providing the neck trunnion with deformable metallic surface ribs, providing a deformable adapter and fitting the adapter over the ribs, providing a trial ball having a non-metallic bore, and including axially forcibly fitting that bore over the deformable adapter to deform the adapter without deforming the ribs, as the trial ball adjustingly arrives at selected axial position on the neck trunnion corresponding to correct position of the trial ball in the socket, and correspondingly subsequent correct axial positioning of the implantable ball on the neck trunnion. | 2013-10-03 |
20130261763 | DEVICES AND METHODS FOR TREATING SLEEP DISORDERED BREATHING - Devices and methods of treating sleep disordered breathing are provided herein. The devices are designed capable of preventing collapse of an oral airway tissue during sleep while maintaining normal velopharyngeal functions. | 2013-10-03 |
20130261764 | MULTIFUNCTIONAL PROSTHESES WITH MULTILAYER COVERING AND METHODS OF PRODUCTION THEREOF - Multifunctional prostheses which include a prosthesis body having at least one interface wall suitable for interfacing with at least one bone tissue, and which also include a substrate are provided. Advantageously, a first covering comprising first functional groups suitable to form chemical bonds, is applied to said substrate. On the side of the first covering the substrate may include protuberances and/or recesses suitable for promoting the attachment of said first functional groups. A second covering comprising nanostructures may be applied to the first covering, on the side opposite the substrate, and an interface covering comprising molecules may be applied to the second covering on the side opposite the first covering. Second functional groups suitable to form chemical bonds, so as to strengthen the bonds between the second covering and the interface covering may be inserted between the interface covering and the second covering. Methods of making such prostheses are also provided. | 2013-10-03 |
20130261765 | BONE REPAIR MATERIAL AND METHOD FOR PRODUCING THE SAME - A bone repair material being superior in apatite-forming ability and its stability in a storage and high in scratch resistance is disclosed. The material is produced by a method comprising the steps of: immersing a substrate made of titanium or a titanium alloy in a first aqueous solution that does not contain calcium ions but contains at least one cation selected from the group consisting of sodium ions and potassium ions and is alkaline; immersing the substrate in a second aqueous solution that does not contain phosphate ions but contains calcium ions; heating the substrate in a dry atmosphere; and treating the substrate with hot water of 60° C. or higher or with steam. | 2013-10-03 |
20130261766 | POWERED PROSTHETIC HIP JOINT - A powered prosthetic thigh can have a proximal portion configured to couple to a prosthetic hip socket and can have a distal portion attached to the proximal portion. The distal portion can have a distal connector configured to couple to a prosthetic knee. The powered prosthetic thigh can also have a computer controlled actuator configured to rotate the prosthetic thigh relative to the prosthetic hip socket. | 2013-10-03 |
20130261767 | FOOT PROSTHESIS - Foot prosthesis, comprising an upper part, and a lower part that is placed on the ground when walking, which parts extend one above the other and at a distance from each other, are connected to each other at the forefoot and the heel and, forming a spring, move relative to each other during walking, wherein the upper part ( | 2013-10-03 |
20130261768 | Light control system and method for automatically rendering a lighting atmosphere - The invention relates to the automatic rendering of a lighting scene with a lighting system, particularly the control of the rendering. A basic idea of the invention is to perform rendering of a lighting scene by decomposing a lighting atmosphere to be rendered in elementary light effects, to classify the elementary light effects, and to coordinate the realisation of the classified light effects with the lighting system. An embodiment of the invention provides a light control system ( | 2013-10-03 |
20130261769 | CONTEXT RECOGNITION APPARATUS AND METHOD - Context recognition methods and apparatus are provided for an application processor and a micro control unit. It is determined whether an operation switch condition for switching to a sleep mode is satisfied. A request for execution of a context recognition function is sent to a micro control unit, when the operation switch condition is satisfied. The application processor switches to the sleep mode, when the context recognition function is executed by the micro control unit. The micro control unit collects sensor data at previously stored time intervals, and previously stored state information is updated based on the sensor data. | 2013-10-03 |
20130261770 | FREQUENCY CONTROL DEVICE, FREQUENCY CONTROL METHOD - The object is to appropriately control a frequency of performing the link process. | 2013-10-03 |
20130261771 | GESTURE CONTROL FOR MONITORING VITAL BODY SIGNS - The present invention reuses an accelerometer, or, more precise, sensed accelerations of a body sensor for user control of the body sensor. This is achieved by detecting predefined patterns in the acceleration signals that are unrelated to other movements of the patient. These include tapping on/with the sensor, shaking, and turning the sensor. New procedures are described that make it possible to re-use the acceleration sensing for reliable gesture detection without introducing many false positives due to non-gesture movements like respiration, heart beat, walking, etc. | 2013-10-03 |
20130261772 | Method and Apparatus for Parameterizing a Safety Device - A method and apparatus for parameterizing a device with parameters from a parameter list, wherein in an event of a match occurring between an external parameter token calculated externally based on the parameter list, and an internal parameter token calculated internally by the device to be parameterized based on the parameter list, an external device token input into the device is compared with an internal device token, which is calculated internally by the device to be parameterized based on a device ID for the device and the internal parameter token to validate the parameter list such that fast and reliable parameterization of a device, particularly a safety critical device, which is provided in an industrial installation or a vehicle, is achieved. | 2013-10-03 |
20130261773 | SUPERVISORY PROCESS CONTROL AND MANUFACTURING INFORMATION SYSTEM APPLICATION HAVING AN EXTENSIBLE COMPONENT MODEL - A template-based supervisory process control and manufacturing information application development facility is disclosed that includes a number of time-saving application development tools that significantly enhance design productivity and allow re-using of previously developed application building blocks. The development facility includes an application object template library that stores a set of previously defined application object templates. The template library is accessed by developers through a configuration utility that facilitates specifying instances of the set of previously defined application object templates to be included in an application. Thereafter, application objects are instantiated from the selected ones of the set of previously defined application object templates in a build of the specified application. | 2013-10-03 |
20130261774 | SECURITY MONITORING SYSTEM AND METHOD - A security monitoring system/method implementing distributed Internet-based environmental monitoring and control is disclosed. The system utilizes a smart gateway power controller (SGPC) configured for new/retrofit installation into electrical power distribution networks to allow controlled connection of an AC power source to a customer load device under direction of local or remote Internet direction. The SGPC may also be configured with sensors to detect motion, audio, video, visual images, smoke, carbon monoxide, carbon dioxide, light/darkness, and other environmental data. The SGPC may be configured using a local web-based graphical user interface (GUI) to relay collected sensor information to a remote web browser hosted on a remote computing device. The GUI may incorporate a configuration/setup interface allowing mapping of sensor data to information associated with the sensor location and triggered security reports to occur based on collected sensor data. | 2013-10-03 |
20130261775 | PACEMAKER APPARATUS, OPERATION METHOD THEREOF, AND PROGRAM - There is provided a pacemaker apparatus including a course setting unit configured to set a movement course along which a user moves, a lap time data acquisition unit configured to acquire data of one or more lap times of one or more persons during movement along the course set by the course setting unit, and a target lap time generation unit configured to designate a lap time of a person selected by the user among the data of the one or more lap times of the one or more persons acquired by the lap time data acquisition unit as a reference lap time and generate a target lap time based on data of the reference lap time. | 2013-10-03 |
20130261776 | SYSTEM AND METHOD FOR GENERATING AND USING CUSTOMIZED ATHLETIC WORKOUTS - A method for generating and using a workout file, comprising recording workout data and notes while performing an athletic workout, attaching trigger conditions to the notes, and exporting the workout data, the notes, and the attached trigger conditions as the workout file, where the exported workout file is configured to be used by a subsequent user to repeat the athletic workout in a manner that plays the notes when the subsequent user performs the trigger conditions. | 2013-10-03 |