Abstract: A stimulation protocol determination system includes an input module and a selector module. The input module is provided to receive an indication of an upper airway flow limitation via sensed respiratory effort information. The selection module is provided to automatically select, based on the indicated upper airway flow limitation, a stimulation protocol.

Abstract: A power element for an implantable medical device is described. The implantable medical device includes sealingly contained circuitry and a sealingly contained power element. The sealingly contained power element supplies power to the circuitry.

Abstract: A system and/or method involving identifying a care usage pattern of an implantable medical device (IMD) for a patient associated with the IMD, and setting a data event parameter for the IMD based on the care usage pattern.

Abstract: An electrode cuff includes a first elongate portion and a second elongate portion. The first elongate portion is configured to removably contact a length of a nerve while the second elongate portion extends outwardly at an angle relative to a first side edge of the first elongate portion to at least partially wrap about the nerve. The electrode cuff includes a first series of electrodes that is spaced apart longitudinally along the first elongate portion. A width of the second elongate portion is sized to fit between adjacent branches extending from a nerve.

Abstract: A system and/or method to treat incontinence of a patient includes a stimulation element implanted to stimulate one or more target sites to activate an external sphincter or other mechanism of continence of the patient, such as the external urethral sphincter and/or the external anal sphincter.

Abstract: Simulation electrode assemblies for applying bilateral stimulation, for example stimulating both the left and right hypoglossal nerves of a patient in the treatment of sleep disordered breathing. In some methods, a stimulation electrode assembly is inserted through an incision at a side of the patient and implanted at a location extending across the patient's mid-line.

Abstract: Methods and systems provide for receiving, at a remote server, first data and a first sharing key acquired from a first processor associated with a first medical practice, and receiving, at the remote server, second data and a second sharing key acquired from a second processor associated with a second medical practice. The methods and systems provide for comparing, by the remote server, the first sharing key to the second sharing key, and granting, to the first and second processors by the remote server, access to the first and second data stored in the remote server in response to a successful comparison of the first and second sharing keys. The methods and systems provide for sharing, by the remote server, the first and second data with the first and second processors in response to the grant of access.

Abstract: A cuff electrode includes at least an array of electrodes to extend circumferentially about a nerve, and methods of making and using a cuff electrode.

Abstract: An apparatus includes an implantable stimulator to treat sleep disordered breathing (SDB) and at least one electrode associated with the stimulator.

Abstract: An electronic medical device includes a first portion, with the first portion including a first insertion hole and an external surface. The first insertion hole is to removably receive an elongate element. The external surface of the first portion comprises a first position indicator, which is located to be visibly juxtaposed relative to a first operative element of the elongate element when the elongate element is fully inserted in the first insertion hole. In some instances, the position indicator may serve a dual function as a vent.

Abstract: A system and method for automatically implementing a therapy for treating sleep disordered breathing.

Abstract: A communication platform at least partially implements secure communications between a medical device and a trusted authority (TA) service provider. The secure communications prevent access to the secure communications by the communication platform while permitting access to the secure communications at the medical device and/or at the trusted authority service provider.