A system and method for allowing any surgeon, including those surgeons who perform a fewer number of a revision procedure as compared to a more experienced surgeon who performs a greater number of procedures, to provide an improved likelihood of a favorable outcome approaching, if not exceeding, a likelihood of a favorable outcome as performed by a very experienced surgeon with the revision procedure. An engine is operable in two distinctive selectable modes including a unidirectional mode providing only extractive forces and a bidirectional mode providing both extractive and insertional forces

An electrolarynx includes tone-producing circuitry, a power switch to turn on the circuitry, a control button (i.e., a pushbutton) to actuate the power switch, a pressure-sensitive-resistor (PSR) that is physically coupled to the pushbutton, and a mode switch. PSR resistance is dependent on the amount of pressure applied to the pushbutton, and the tone-producing circuitry is configured to respond to such variations in PSR resistance according to a user-selected mode of electrolarynx operation set by operation of the mode switch. Said modes preferably include multiple frequency-varying modes (FVMs) in which the frequency of the electrolarynx tone is varied with different sensitivities to variations in PSR resistance, and multiple volume-varying modes (VVMs) having different sensitivities. A preferred embodiment also includes a communications-link mode, for receiving control information from an external device, and a disabled mode. Preferably, the tone-producing circuitry includes a microcontroller component that is configured for electrolarynx operation under program control.

The present disclosure provides implants, sensor modules, networks, and methods configured to establish transcutaneous power and transcutaneous bidirectional data communication using ultrasound signals between two or more medical devices located on and within a body of a patient.

The present disclosure provides implants, sensor modules, networks, and methods configured to establish transcutaneous power and transcutaneous bidirectional data communication using ultrasound signals between two or more medical devices located on and within a body of a patient.

Provided herein are cranial implant devices that include at least one acoustic, optical, and/or photoacoustic lens element comprising one or more electromagnetically translucent, electromagnetically transparent, sonolucent, and/or acoustically active materials. The cranial implant devices are structured for subgaleal scalp implantation within, beneath, and/or over at least one cranial opening of a subject and typically includes a substantially anatomically-compatible shape. In addition, the cranial implant devices permit transcranial therapeutic ultrasound, transcranial diagnostic ultrasound, photoacoustic imaging, electromagnetic wave diagnostic imaging, and/or electromagnetic wave therapeutic intervention of intracranial matter of the subject via the acoustic, optical, and/or photoacoustic lens element when the cranial implant device is subgalealy implanted within, beneath, and/or over the cranial opening of the subject. Other aspects are directed to various related systems and methods of obtaining diagnostic information from, and/or administering therapy to, a subject.

An exemplary device (e.g., an intravascular prosthesis) can be provided which can comprise an expandable configuration (e.g., a housing) configured or structured to be inserted within a luminal biological structure (e.g., a blood vessel). The expandable configuration can include at least one self-expanding system which is (i) a wire system and/or a mesh system, and (ii) configured to include a plurality of apical connectors, a subset thereof connecting to a medial structure. The expandable configuration can also include at least one flexible interconnect system configured or structured to house (i) at least one integrated circuit, (ii) at least one electrode, and (iii) at least one transducer. Alternatively or additionally, the expandable configuration can comprise a medial structure connected to one or more of the apical connectors, and which is be dissolved within the tubular biological structure to nontoxic species over a controlled time frame. Exemplary methods can also be provided for installing such exemplary intravascular prosthesis within a luminal biological structure.