Abstract: Sound processing strategies for use with cochlear implant systems utilizing simultaneous stimulation of electrodes are provided. The strategies include computing a frequency spectrum of a signal representative of sound, arranging the spectrum into channels and assigning a subset of electrodes to each channel. Each subset is stimulated so as to stimulate a virtual electrode positioned at a location on the cochlea that corresponds to the frequency at which a spectral peak is located within an assigned channel. The strategies also derive a carrier for a channel having a frequency that may relate to the stimulation frequency so that temporal information is presented. In order to fit these strategies, a group of electrodes is selected and the portion of the current that would otherwise be applied to electrode(s) having a partner electrode in the group is applied to the partner electrode.

Abstract: An adaptive place-pitch ranking procedure for use with a cochlear implant or other neural stimulation system provides a systematic method for quantifying the magnitude and direction of errors along the place-pitch continuum. The method may be conducted and completed in a relatively short period of time. In use, the implant user or listener is asked to rank the percepts obtained after a sequential presentation of monopolar stimulation pulses are applied to a selected spatially-defined electrode pair. Should the patient's judgment of pitch order be correct for all applied interrogations, then no further testing involving the tested electrode pair (two electrode contacts) is undertaken. However, should there be errors in the place-pitch ranking, which errors evidence perceptual place-confusions, then a search is undertaken for the spread of the perceptual confusion by separating the target channel and competing channel by one electrode contact at a time.

Abstract: A hearing device fitting device that includes a computing device (3), connected on an input side with a connection (E3) for data entry and on an output side with a connection (A3) for a hearing device. The hearing device fitting device further includes an audio storage medium play-back unit having a control input (E9) connected to a computing device (3) output and having an audio output (A3) connectable to a loud speaker unit (11) input. The device supports a method a method for fitting the hearing device in situ by applying the hearing device to an individual; subjecting the individual to an audio test signal; having the individual appraise said audio test signal; and automatically selecting, in dependency of said appraising, a subsequent audio test signal.

Abstract: Methods of denoising a neural recording signal include correlating a neural recording signal with a number of basis functions to obtain a number of weights and then multiplying the weights with the basis functions to obtain a denoised neural recording signal. The basis functions are derived using principal component analysis. Systems for denoising a neural recording signal include one or more devices configured to correlate a neural recording signal with the basis functions to obtain the weights and then multiply the weights with the basis functions to obtain the denoised neural recording signal.

Abstract: Method for accurately measuring hearing loss includes the steps of selecting a series of audio tones within the normal range of hearing (502) and then measuring a relative sensitivity of a test subject with respect to the ability to hear each of the audio tones, exclusive of the effects of tinnitus. (504, 506, 508, 510, 512) The relative sensitivity of the test subject to hear the tones can be measured by determining (510) for each tone an intensity necessary for the test subject to hear the tones at a subjectively equal loudness level which is selected to exceed a perceived level of noise attributable to tinnitus for the test subject.

Abstract: A method for correcting sound for the hearing impaired includes analyzing an incoming sound into frequency channels and computing a group delay of each of the frequency channels that is expected in a healthy ear. A correction is defined as a percentage less than 100% of the group delay (GD) that a given impaired ear has compared to the group delay of the healthy ear. The amount of delay for the correction as a function of time is computed for each frequency channel, which delay is imposed on each frequency channel. The signal levels are scaled to adjust for audibility, after which the delayed and scaled signals from all frequency channels are combined into an outgoing sound.

Abstract: An implant device for bone anchored hearing aids of the type that include a screw-shaped anchoring element for anchorage in the bone tissue, an abutment sleeve for skin penetration and arranged to be connected to the fixture with a screw connection and a tool for installing the implant into the bone tissue. The fixture and the abutment sleeve are made as a pre-mounted unit that unit is arranged to be installed in one step by means of the tool, which is arranged to cooperate with a tool engaging portion on the abutment sleeve. This arrangement requires fewer pieces to handle for the surgeon during the installation, which means that the surgical procedure can be carried out in a simpler and predetermined way, at the same time as the advantages inherent in a two-piece implant device are maintained.

Abstract: An implantable cochlear implant electrode array (30) that can adopt a first, preferably straight, configuration selected to allow the array to be inserted into the cochlea and at least a second, preferably, spirally curved, configuration wherein the electrode array (30) is adapted to apply tissue stimulation. The electrode array (30) comprises an elongate carrier (31) having a proximal end (37), a distal end (34), and a plurality of electrodes supported by the carrier (31) at respective spaced locations thereon, the carrier (31) is formed, preferably moulded, to preferentially adopt the second configuration or another configuration different to said first configuration. The outer layer (33) is releasably connected to the elongate carrier (31) by an adhesive layer (32) and is formed so as to bias the carrier (31) into the first configuration when connected thereto. A method of forming the electrode array (30) is also disclosed.

Abstract: A cochlear implant sound processor is powered by a rechargeable battery that is permanently integrated into the sound processor. The sound processor contains an inductive coil that may be tuned to an external charging coil for battery recharging. The electronic circuits and coil of the sound processor are housed in a material transparent to RF signals. The sound processor may be placed in a recharging base station in which the sound processor is positioned in a space surrounded by the inductive charging coil embedded in a material transparent to RF signals. The inductive charging coil sends power to the coil inside the processor and thereby recharges the battery. An alternative embodiment utilizes contacts in the sound processor case and aligned terminals in the recharging base station that allow direct charging of the battery.

Abstract: A method for stimulating nerve or tissue fibers and a prosthetic hearing device implanting same. The method comprises: generating a stimulation signal comprising a plurality of pulse bursts each comprising a plurality of pulses; and distributing said plurality of pulse bursts across one or more electrodes each operatively coupled to nerve or tissue fibers such that each of said plurality of pulse bursts delivers a charge to said nerve or tissue fibers to cause dispersed firing in said nerve or tissue fibers.

Abstract: A sound sensed electric stimulation control device comprises a body. The body further comprises a signal analysis unit for receiving sound signals and converting the signals into output signals; and an electronic stimulation output portion for generating corresponding output energy according to the output signals. The output emerge is controlled by the inputted sound signals to the signal analysis unit. The signal analysis unit is connected to a signal input unit. The signal analysis unit is connected to a sound input unit. The signal analysis unit is connected to a built-in sound input unit. The signal analysis unit includes a frequency band energy detector, a detected energy identifier and an electronic stimulation control unit so as to analyze features of inputted sound signals and then convert the sound signals into output signals so as to stimulate the electronic stimulation output portion to output energy.

Abstract: A telemetry antenna for an implantable medical device includes one or more portions having a non-linear configuration. In some embodiments, the non-linear configuration provides an antenna having a greater antenna length than the linear lengthwise dimension of the antenna structure. In some embodiments, the non-linear configuration is a serpentine pattern.

Abstract: A system and method for preserving temporal and spatial resolution in complex sounds for poor performing patients having high stimulation thresholds is described. The system and method employs two or more adjacent electrode contacts to deliver concurrent stimulation. This concurrent delivery of stimuli creates a high current field intensity that overlaps between individual current fields generated by the two or more adjacent electrodes and which individual fields are summed to create an overlapping field that has a higher current field intensity than a single current emanating from an individual electrode. The use of this method reduces or eliminates the need to increase either the stimulus current amplitude or to increase the pulse width, both of which may cause loss of system resolution, i.e., loss of fine structure information that is used to resolve complex sounds such as music.

Abstract: According to one aspect, an electrical stimulation system for treating tinnitus is provided. The system includes an electrical stimulation lead adapted for implantation into the person's skull for electrical stimulation of target brain tissue located in the person's temporal lobe. The lead includes one or more electrodes adapted to be positioned near the target brain tissue and to deliver electrical stimulation energy to the target brain tissue. The system also includes a stimulation source operable to generate signals for transmission to the electrodes of the lead to cause the electrodes to deliver electrical stimulation energy to the target brain tissue located in the person's temporal lobe to reduce tinnitus effects.

Abstract: There is provided a method for providing hearing assistance to a user, comprising: capturing audio signals by a microphone arrangement (18) and transmitting the audio signals by a transmission unit (10) via a modulated wireless audio link (30) to a receiver unit (12) and receiving the audio signals at the receiver unit (12); analyzing the amplitude of the received audio signals by an analyzer unit (34) of the receiver unit (12); dynamically adjusting by a gain control unit (36) located in the receiver unit (12) the gain applied to the received audio signals according to the result of the analysis by the analyzer unit (34), wherein the gain is equal to or larger than a first value (GH) if the amplitude of the received audio signals is equal to or larger than a first threshold (U1H) and is reduced to a finite value less than said first value if the amplitude of the received audio signals is less than said first threshold (U1H); and stimulating the user's hearing by stimulating means (14, 16) worn at or in the u

Abstract: There is provided a method for adjusting a system for providing hearing assistance to a user (101), the system comprising a microphone arrangement (26) for capturing audio signals, a transmission unit (102) for transmitting the audio signals via a wireless link (107) to a receiver unit (103) worn by the user, a gain control unit (126) located in the receiver unit for setting the gain applied to the audio signals, and means (38) worn at or in a user's ear (39) for stimulating the hearing of the user according to the audio signals from the receiver unit (103), said method comprising: generating test audio signals, transmitting said test audio signals at a pre-defined level from the transmission unit via the wireless link to the receiver unit and stimulating the user's hearing with said test audio signals via said stimulating means; simultaneously transmitting gain control commands from the transmission unit to the gain control unit in order to selectively change the gain set by the gain control unit; repeating

Abstract: Objectively measuring tinnitus in human and animal subjects. A subject is exposed to an alteration in a sound pattern otherwise qualitatively similar to the subject's tinnitus and a startle reflex is induced. The subject's acoustic startle response is obtained and used to determine whether the subject detected the alteration of the sound pattern.

Abstract: An exemplary method of fitting a coeblear implant system to a patient includes establishing an implant fitting line having a slope and a position. The implant fitting line represents a relationship between a number of stimulation sites within a cochlea of the patient and a number of corresponding audio frequencies. That is, the implant fitting line defines which locations along the length of the cochlea, when stimulated, are perceived by the patient as specific tones or frequencies. The method further includes presenting a first audio signal having a number of audio frequencies to the patient and applying a stimulus current to one or more stimulation sites corresponding to the number of audio frequencies of the first audio signal. The method further includes adjusting the slope of the fitting line based on a response of the patient to the stimulus current.

Abstract: A method and device are disclosed for neural stimulation with improved power consumption and/or effectiveness. The stimulus generator is arranged, for example via a look up table, to recognize proposed stimuli which will be masked by earlier or simultaneous stimuli. Such masked stimuli are either deleted, or replaced by another stimulus.

Abstract: A cochlear implant electrode assembly device (10) comprising an elongate electrode carrier member (11), a first stiffening element (15a), and a second stiffening element (15b). The carrier member (11) is made of a resiliently flexible first material and has a plurality of electrodes (12) mounted thereon. The carrier member (11) has a first configuration selected to allow it to be inserted into an implantee's cochlea (30), a second configuration wherein it is curved in shape to match a surface of the cochlea (30), and at least one intermediate configuration between the first and second configurations. Both the first and second stiffening elements (15a, 15b) are made of a material relatively stiffer than said the material and in combination bias the elongate member into the first configuration. If either the first stiffening element (15a) or the second stiffening element (15b) are removed, the elongate member (11) adopts the at least one intermediate configuration.

Abstract: Errors in pitch (frequency) allocation within a cochlear implant are corrected in order to provide a significant and profound improvement in the quality of sound perceived by the cochlear implant user. In one embodiment, the user is stimulated with a reference signal, e.g., the tone “A” (440 Hz) and then the user is stimulated with a probe signal, separated from the reference signal by an octave, e.g., high “A” (880 Hz). The user adjusts the location where the probe signal is applied, using current steering, until the pitch of the probe signal, as perceived by the user, matches the pitch of the reference signal, as perceived by the user. In this manner, the user maps frequencies to stimulation locations in order to tune his or her implant system to his or her unique cochlea.

Abstract: A middle ear prosthesis comprises a one piece disk shaped prosthesis including a generally circular malleable body including a bore. The body engages a tympanic membrane and the bore receives a head of a stapes when implanted in a middle ear. More particularly, the middle ear prosthesis comprises a body comprising an annular head, a collar, and a plurality of radially extending members connecting the head to the collar. The head engages a tympanic membrane and the collar receives a head of a stapes when implanted in a middle ear.

Abstract: A status indicator is provided for use with a medical device that employs a power transmitting coil. In one embodiment, the status indicator comprises a receiving coil and feedback element. The feedback element, such as a light emitting diode (LED) or liquid crystal display (LCD), is electrically coupled to the receiving coil. In another embodiment a status indicator is incorporated into the medical device, which status indicator comprises a feedback element and electronic circuitry for detecting device function and program selection. The circuitry and feedback element are incorporated into the medical device such as on the earhook of a behind-the-ear (BTE) hearing device.

Abstract: Contrast between various frequency components of sound is enhanced through a lateral suppression strategy to provide increased speech perception in the electrically stimulated cochlea. A received audio signal is divided into a plurality of input signals, wherein each input signal is associated with a frequency band. A plurality of envelope signals are generated by determining the envelope of each of a plurality of the input signals. At least one of the envelope signals is scaled in accordance with a scaling factor to generate at least one scaled envelope signal. An output signal is generated by combining at least one envelope signal with at least one scaled envelope signal, and the cochlea is stimulated based on the generated output signal. The lateral suppression strategy can be applied to one or more frequency bands using scaled amplitude signals associated with one or more neighboring frequency bands.

Abstract: An auditory prosthesis includes an implanted component and an external component. The external component includes a transmitter for transmitting electromagnetic signals to the implanted component; means for detecting electromagnetic emissions of the transmitter; and means for indicating when the electromagnetic emissions of the transmitter have been detected.

Abstract: A system for treating patients affected both by hearing loss and by balance disorders related to vestibular hypofunction and/or malfunction, which includes sensors of sound and head movement, processing circuitry, a power source, and an implantable electrical stimulator capable of stimulating areas of the cochlea and areas of the vestibular system.

Abstract: A repeater device allows a remote unit to control, program and/or monitor a medical implant device from a much further distance than has heretofore been possible. Such repeater device also facilitates transmitting other signals, i.e., other than control signals, to the medical implant device, such as, e.g., streaming audio, or other auxiliary input data. In one embodiment, the repeater device also allows status signals or sensed data originating within the medical implant device to be transmitted from the medical implant device through the repeater device to the remote unit, even though the remote unit may be located some distance, e.g., up to 200 feet, from the medical implant device. Such transmitted signals when received at the remote unit may be processed, analyzed, stored, monitored and/or displayed.

Abstract: A cochlear implant wherein the return path of the electrode array is located to increase current flow through the modiolus. The return electrode is placed at various locations outside the cochlea, and into the modiolus itself. In addition, the electrode array includes an inflatable membrane that is inflated to anchor the array in position in the cochlea with the electrode contacts pressed into contact with the modiolar wall and allowing the membrane to seal with the surrounding tissue of the cochlea, increasing the longitudinal resistance along the cochlear implant electrode, decreasing shunting of the injected current via scala tympani. In experiments that were conducted the current along the modiolus was determined to be, on average, 2.4 times larger with the return electrode in the modiolus than in an extracochlear location.

Abstract: A cochlear implant electrode assembly device (10) comprising an elongate electrode carrier member (11), a stiffening element (15), and a stiffening sheath (16) that at least partially envelops the elongate member (11). The member (11) is made of a resiliently flexible first material and has a plurality of electrodes (12) mounted thereon. The member (11) has a first configuration that allows it to be inserted into an implantee's cochlea (30). The member (11) also has a second configuration wherein the member is curved to match an inside surface of the cochlea (30), and at least one intermediate configuration between the first and second configurations. Both the stiffening element (15) and sheath (16) are made of a material that is relatively stiffer than the member (11). The stiffening element (15) and the stiffening sheath (16) in combination bias the elongate member (11) into the first configuration.

Abstract: A quick-connect system for mechanically and electrically connecting two components therebetween. In an exemplary embodiment, the mechanical quick-connect is comprised of: a receptacle in the first component; a barrel protruding from the second component; and a lock for locking the barrel inside the receptacle. Electrical connection, such as a coaxial connection, can also be obtained between the barrel and receptacle, while in the locked position by using a pin assembly axially located in the barrel. The lock may comprise a tooth and slot configuration, wherein the tooth is in compressive contact with a spring which compression continuously exerts force on the tooth and causes the end of the tooth to engage to the cam slot on the barrel, thereby locking the barrel inside the receptacle. The barrel may be disengaged with a turn that is less than 180 degrees.

Abstract: An implantable neural stimulation system, such as a cochlear implant system, utilizes a Distributed Compression Amplitude Mapping (DCAM) system to distribute signal compression between a pre-bandpass linear mapping function, and a post-bandpass compressive mapping function. The pre-bandpass linear mapping function is implemented, in one embodiment, as a traditional fast audio compressor to prevent distortion that might result from a non-linear mapping. The post-bandpass compressive mapping function is implemented, in one embodiment, as a logarithmic transform to reflect natural hearing. As a result of the DCAM processing, the differences in amplitudes of components of the acoustic spectrum are maintained. By maintaining these differences, spectral smearing between channels is reduced and speech clues are preserved.

Abstract: Improved skipping strategies for cochlear or other multi-channel neural stimulation implants selects N out of M channels for stimulation during a given stimulation frame. A microphone transduces acoustic energy into an electrical signal. The electrical signal is processed by a family of bandpass filters, or the equivalent, to produce a number of frequency channels. In a first embodiment, a probability based channel selection strategy computes a probably for each of the M channels based on the strength of each channel. N channels are probabilistically selected for stimulation based on their individual probability. The result is a randomized “stochastic” stimulus presentation to the patient. Such randomized stimulation reduces under representation of weaker channels for steady state input conditions such as vowels. In second, third and fourth embodiments, a variable threshold is adjusted to obtain the selection of N channels per frame.

Abstract: A system for monitoring and controlling power demands in devices with DC power supplies. In response to a detected decline in voltage levels, the device reduces power demands of the device, in one or more stages before powering down entirely. This approach has application to battery powered devices, particularly fro medical applications such as cochlear implants.

Abstract: A hand-held remote unit functions as both a remote status device and a control device for a cochlear implant system. When placed near the headpiece of a cochlear implant system, the remote unit monitors the forward telemetry signal transmitted between an external speech processor, e.g., a behind-the-ear (BTE) speech processor, and an implanted unit, thereby providing the remote unit with the ability to output status information regarding the system. The remote unit may also generate a back telemetry signal that when properly received by the speech processor causes a forward telemetry signal to be generated that controls the implant unit.

Abstract: A method of programming a bionic ear cochlear implant provides access to the full functionality of the implant, while still providing a simple-to-administer, more reliable, and faster fitting experience for the patient and clinician. The method includes (a) conducting a pre-evaluation stage focused on sorting and identifying bad electrode contacts, reducing fitting time and improving patient performance; (b) conducting a programming stage wherein T and M levels are adjusted based on information derived during the pre-evaluation stage; and (c) conducting a post-evaluation stage wherein wired speech understanding tests are automatically run in order to provide an objective programming choice. The pre-evaluation stage automatically runs a set of objective tests, and then, based on the result of such tests, generates a template for the clinician to use during the programming stage. The objective tests, inter alia, identify and remove bad electrode contacts from the template.

Abstract: An adaptive place-pitch ranking procedure for use with a cochlear implant or other neural stimulation system provides a systematic method for quantifying the magnitude and direction of errors along the place-pitch continuum. The method may be conducted and completed in a relatively short period of time. In use, the implant user or listener is asked to rank the percepts obtained after a sequential presentation of monopolar stimulation pulses are applied to a selected spatially-defined electrode pair. Should the patient's judgment of pitch order be correct for all applied interrogations, then no further testing involving the tested electrode pair (two electrode contacts) is undertaken. However, should there be errors in the place-pitch ranking, which errors evidence perceptual place-confusions, then a search is undertaken for the spread of the perceptual confusion by separating the target channel and competing channel by one electrode contact at a time.

Abstract: An automated method for treating tinnitus by habituation through use of neurological feedback, comprising the steps of connecting a subject through a set of attached headphones to an electronic sound player that is connected to a PC workstation presenting sound examples by software to the subject who can refine them by manipulating a series of controllers on the player, making an electronic recording of the sound in a digital music format, storing the recording in the computer, transferring a copy of the electronic sound file to the subject's electronic music player, generating an EEC signature of the subject's brain activity in response to the presented sound, sound using the customized sound to stimulate the auditory system while the brain activity is recorded, wherein the computer continuously monitors for the feedback signatures and drives the sound stimuli appropriately.

Abstract: The sound processor and method uses a model of basilar membrane motion to select stimuli, based upon the predicted motion which the acoustic signal presented would produce in an acoustically excited normally hearing cochlea. The filter; used, in contrast to single channel per electrode approaches, cover multiple channels and overlap with each other. Consequently the stimuli presented produce a neural excitation pattern which approximates the spatio-temporal travelling wave observed on the basilar membrane in an acoustically excited normally hearing cochlea. Preferably, the predicted electrode stimuli are based upon the instantaneous predicted amplitude of the electrode location.

Abstract: A cochlear implant system, or other neural stimulation system, has the capability to stimulate fast enough to induce stochastic neural firing so as to restore “spontaneous” neural activity. The stimulation rate applied to the more distally-located electrodes of an electrode array connected to the implant system is reduced from the stimulation rate applied to the more proximally-located electrodes. Thus, in the case of a cochlear implant system, the apically-located regions within the cochlea are stimulated at a reduced rate in order to conserve power. Pulse widths of the reduced-rate pulses may further be increased, and amplitudes reduced, to further conserve power. As needed, a low-level random conditioner stimulation signal may be applied to the apical regions of the cochlea in order to ensure the occurrence of random neural firings.

Abstract: A middle ear prosthesis comprises a piston adapted to extend through an oval window when implanted in a human ear. A pair of jaws engage an ossicle when implanted in a human ear. A spring is coupled to the jaws for biasing the jaws toward one another to provide clamping pressure. The jaws are in turn connected to the piston.

Abstract: A method is described to allow for better selection of electrodes for neural stimulation, for example in a cochlear implant. A series of stimuli, at different stimulation levels, are provided at each electrode to be tested, and the neural response to each stimulus is measured, using an implanted electrode. A value is then calculated relating stimulus level to response, to allow the relative responsiveness of electrodes to be determined. This can then be used as the basis for a stimulation map used to select which electrodes are stimulated and at what level.

Abstract: A apparatus and method for inner ear implants is provided that generates signal processing stochastic independence activity across the excited neural population. A high rate pulse train can produce random spike patterns in auditory nerve fibers (hereafter “pseudospontaneous activity”) that are statistically similar to those produced by spontaneous activity in the normal auditory nerve. We call this activity “pseudospontaneous”. Varying rates of pseudospontaneous activity can be created by varying the intensity of a fixed amplitude, high rate pulse train stimulus, e.g., 5000 pps. The high rate pulse train can desynchronize the nerve fiber population and can be combined with a data signal in an inner ear implant. The pseudospontaneous activity can enhance neural representation of temporal detail and dynamic range with an inner ear implant such as a cochlear implant. The pseudospontaneous activity can further eliminate a major difference between acoustic-and electrical-derived hearing percepts.

Abstract: The invention is a method for increasing the airflow to a zinc-air battery such that the energy density is 500 mwh/cc to 1000 mwh/cc. This allows 8 to 16 hours use as a primary (throw-away) battery, with, for example, high-duty cycle, high-drain cochlear implants, and neuromuscular stimulators for nerves, muscles, and both nerves and muscles together. The systems incorporating the high energy density source are also part of the invention, as well as the resulting apparatus of the method. The uses of this inexpensive, i.e., a $1.00 per day, throw-away primary battery are new uses of the modified zinc-air battery and are directed toward helping people hear again, walk again, and regain body functionality which they have otherwise lost permanently.

Abstract: A noninvasive method and system are provided for assessing the performance of implanted actuators of semi or fully-implantable hearing aid systems. The invention utilizes an externally positioned test measurement device to obtain measurements of the electrical impedance of an implanted actuator when driven by a test signal of predetermined characteristics. In one embodiment, the test measurement device may comprise a signal generator for generating the test signal for the actuator, a signal processing unit to compute the electrical impedance from voltage and current measurements, and a user interface to provide an output that is usable to asses the performance of the actuator. The electrical impedance is computable from the voltage and current of the signal passing through the actuator. The electrical impedance is directly related to the mechanical impedance present at the interface between the actuator and middle ear of a patient.

Abstract: An implantable tissue-stimulating prosthesis such as a cochlear implant system comprising an elongate carrier member having a distal end, a proximal end, and at least one electrode positioned thereon; at least one electrical conductor extending from one or more of the at least one electrode; a lead extending from the carrier member and enclosing the at least one electrical conductor; and a holding member constructed and arranged to radially extend outwardly from the surface of the carrier member to facilitate grasping of the holding member during implantation of the carrier member in a patient.

Abstract: In a cochlear implant system, the implantable stimulator includes a monitor which monitors parameters associated with the stimulation signals and/or the power stored in an energy storage element which stores energy transmitted from the processor. This parameter or parameters is/are analyzed and one or more feedback signals are generated and transmitted back to the processor. The processor uses the feedback signal to insure that power is transmitted to the stimulator optimally and that the stimulation signals are compliant.

Abstract: A middle ear prosthesis comprises a piston adapted to extend through an oval window when implanted in a human ear. A pair of jaws engage an ossicle when implanted in a human ear. A spring is coupled to the jaws for biasing the jaws toward one another to provide clamping pressure. The jaws are in turn connected to the piston.

Abstract: An envelope based amplitude mapping achieves the signal compression required to provide a natural sound level without the high processor loading or waveform alteration. In a preferred embodiment, the output of a family of parallel bandpass filters is processed by an envelope detector, followed by decimation. The resulting reduced data rate envelope is log mapped to produce a scaling factor for the original high data rate bandpass filter output sequence. The resulting scaled signal determines the current level for stimulation of the cochlea for each frequency band, which stimulation achieves a log mapping of the sound amplitude effect similar to natural hearing, while reducing processor load, and preserving waveform shape.

Abstract: A system for treating various neurological, vestibular, and other disorders includes a stimulator device situated in an ear canal of the patient. The stimulator device is adapted to provide magnetic, electrical, audible, tactile, or caloric stimulation, and may be programmed to provide such stimulation in continuous, semi-continuous, periodic, programmed, or on-demand modes, or various combinations of the above.

Abstract: A system and method for application of pseudospontaneous neural stimulation is provided that can generate stochastic independent activity across an excited nerve or neural population without an additional disadvantageous sensations. High rate pulse trains, for example, can produce random spike patterns in auditory nerve fibers that are statistically similar to those produced by spontaneous activity in the normal ear. This activity is called “pseudospontaneous activity”. Varying rates of pseudospontaneous activity can be created by varying the intensity of a fixed amplitude, high rate pulse train stimulus, e.g., 5000 pps. A method and apparatus for diagnosing treatment for tinnitus with neural prosthetic devices according to the present invention that can use, for example, physiological responses to pseudospontaneous activity in an auditory nerve prior to the implementation of the neural prosthetic.