Abstract: An active implantable medical device (AIMD) assembly has a medical device housing containing an electrical power source connected to control circuitry, and a header assembly connected to the device housing. The header assembly supports a plurality of co-axially aligned terminal blocks that are in open communication with a header opening. A conventional strain relief member is connected to the header assembly at the header opening. A number of different auxiliary strain relief devices are described. The auxiliary strain relief devices connect to the conventional strain relief member to help reduce tension and stress on a lead after the AIMD assembly is implanted in a body and the lead electrodes are connected to body tissue.

Abstract: An active medical device has a feedthrough with at least two terminal pins that are connected to electronic components in the device housing. A lead connector is connected to a strain-relief device for a lead. The lead connector supports at least two connector pins that are detachably connected to the device terminal pins to thereby connect the device electronic components to the lead electrodes. The device housing has a length extending along a longitudinal axis, and secondary axes of the terminal pins connected to the connector pins are aligned parallel to the longitudinal axis. The feedthrough also has spaced-apart distally extending arms with detents, and the lead connector has spaced-apart lateral recesses. With the detents of the feedthrough arms received in the lateral recesses of the lead connector, the medical device is detachably connected to the strain-relief device and the lead.

Abstract: An active medical device has a feedthrough with at least two terminal pins that are connected to electronic components in the device housing. A lead connector is connected to a strain-relief device for a lead. The lead connector supports at least two connector pins that are detachably connected to the device terminal pins to thereby connect the device electronic components to the lead electrodes. The device housing has a length extending along a longitudinal axis, and secondary axes of the terminal pins connected to the connector pins are aligned parallel to the longitudinal axis. The feedthrough also has a hub that extends distally from the body fluid side end surface of the ferrule. The hub has an opening. The lead connector has an inlet with inlet opening. A screw in the hub and inlet openings secures the medical device to the lead connector, the strain-relief device, and the lead.

Abstract: An active medical device has a feedthrough with at least two terminal pins that are connected to electronic components in the device housing. A lead connector is connected to a strain-relief device for a lead. The lead connector supports at least two proximally-facing C-shaped inserts with an annular spring nested therein that are detachably connected to the device terminal pins to thereby connect the device electronic components to the lead electrodes. The device housing has a length extending along a longitudinal axis, and secondary axes of the terminal pins connected to the C-shaped inserts/annular springs are aligned parallel to the axis with imaginary extensions of the connector axes extending into the device housing.

Abstract: In various examples, an enclosure for an implantable medical device includes a first enclosure portion and a second enclosure portion, wherein at least the first enclosure portion and the second enclosure portion are joined together to form the enclosure. At least one feature is configured for attachment of at least one component of the implantable medical device to the enclosure. The at least one feature is integrally formed with the enclosure. In some examples, the enclosure is formed by machining.

Abstract: An implantable neural stimulation device is provided, comprising a body containing stimulation electronics, and a battery to provide stimulation energy, a lid, coupled to the body, the lid configured to at least partially seal the body and a header coupled to the body of the device. The header comprises a contact assembly electrically coupled to the stimulation electronics via at least one feedthrough wire extending through the lid, the contact assembly configured to connect to a stimulation lead to deliver the stimulation energy from the battery under control by the stimulation electronics, a charge coil configured to charge the battery, and a support component configured to support the charge coil. The support component is supported in position by the contact assembly.

Abstract: An active implantable medical device (AIMD) has an alumina housing supporting at least two electrodes. A printed circuit board (PCB) assembly resides inside the housing. Two sintered platinum-containing pathways extend through the housing thickness from the electrodes supported on the housing body fluid side surface to a housing device side surface. A device side end of each of the two platinum-containing pathways is in electrical continuity with an electrical contact supported on the PCB to energize the electrodes for providing stimulation therapy to a patient or for sensing biological signals from the patient.

Abstract: An inductive charging antenna for charging the power source of an active implantable medical device (AIMD) is described. The charging antenna is supported on the body fluid side of the feedthrough insulator, on the device side of the insulator or it is embedded inside the insulator. The charging antenna is connected to electronic circuits housed inside the medical device to charge the power source so that the device can deliver electrical stimulation to a patient and receive sensed biological signals from body tissue, among other functionalities. If the charging antenna is supported on the insulator body fluid side, it is made from a biocompatible material such as platinum. However, if the charging antenna is embedded inside the feedthrough insulator or is supported on the device side of the insulator, it can be made from a less expensive material that is not biocompatible, for example, copper.

Abstract: In various examples, a connector for an implantable medical device is configured to accept a lead therein and electrically couple to a lead contact of the lead. The connector includes a connector housing, which includes a bore portion including a bore hole therethrough. The bore hole includes a bore hole axis, the bore hole being sized and shaped to accept the lead within the bore hole. An attachment portion is coupled to the bore portion. The attachment portion includes an attachment hole within the attachment portion sized and shaped to accept a feedthrough wire within the attachment hole. The attachment hole includes an attachment hole axis offset from and non-parallel to the bore hole axis.

Abstract: A lead adapter for a patient treatment system comprises a housing having a plurality of inlets, each inlet being segregated from an immediately adjacent inlet by a housing intermediate wall. A plurality of electrical contact assemblies residing in the housing are electrically connected to a respective one of a plurality of electrical contact posts. Each contact post has an exposed terminal portion residing in one of the plurality of inlets. A header is movably secured to the housing to selectively open and close the housing. With the header in an open position, an implantable lead is movable into a longitudinally extending opening in the header. The header is then manipulatable into a closed position to move an electrical contact of the lead into contact with a respective one of the electrical contact assemblies electrically connected to a respective one of the electrical contact posts.

Abstract: A device that is implantable in body tissue of a human or animal. The device is comprised of a header comprising at least one terminal adapted for removable connection to a lead and an open ended case closed by a plate to form a housing. The housing is comprised of a surrounding edge wall joined to a first side wall and a second side wall opposed to the first side wall. At least a first suture port extends through the edge wall and the second side wall but not the first side wall at an upper edge region of the housing. A second suture port may extend through the surrounding edge wall and the second side wall but not the first side wall in a similar manner. A third suture port may extend through the header. The three suture ports may define a triangular attachment configuration.

Abstract: In various examples, a header of an implantable device includes a first header portion and a second header portion at least partially disengageable from the first header portion. In a closed configuration, the first header portion is fully engaged with the second header portion, and in an open configuration, the first header portion is at least partially disengaged from the second header portion. At least one bore within the header is sized and shaped to accommodate a proximal end of a lead. The bore is split substantially longitudinally to form a first bore portion and a second bore portion. With the proximal end of the lead disposed within the bore and a positioning feature interacting with a lead feature, at least one lead contact aligns with at least one header contact to allow the at least one lead contact to electrically couple to the at least one header contact.

Abstract: A device that is implantable in body tissue of a human or animal. The device is comprised of a header comprising at least one terminal adapted for removable connection to a lead and an open ended case closed by a plate to form a housing. The housing is comprised of a surrounding edge wall joined to a first side wall and a second side wall opposed to the first side wall. At least a first suture port extends through the edge wall and the second side wall but not the first side wall at an upper edge region of the housing. A second suture port may extend through the surrounding edge wall and the second side wall but not the first side wall in a similar manner. A third suture port may extend through the header. The three suture ports may define a triangular attachment configuration.

Abstract: A cable assembly for a patient treatment system comprises an electrical cable having a proximal connector configured to connect to an external electrical stimulator device and a distal connector including a distal housing having an open distal end. The distal housing houses a manifold that supports a plurality of spring-loaded electrical contact assemblies aligned in two rows and being electrically connected to a corresponding one of a plurality of electrical contacts in the proximal connector. The housing distal open end is closed by a header that is movable between a closed position resting on the housing open end and an open position spaced there above. The header has a pair of side-by-side longitudinally extending openings. With the header in the open position, a practitioner holds the distal connector in one hand and with the other hand inserts the distal electrical contacts of one or two therapy delivery devices into the longitudinally extending openings.

Abstract: A cable assembly for a patient treatment system comprises an electrical cable having a proximal connector configured to connect to an external electrical stimulator device and a distal connector including a distal housing having an open distal end. The distal housing houses a manifold that supports a plurality of spring-loaded electrical contact assemblies aligned in two rows and being electrically connected to a corresponding one of a plurality of electrical contacts in the proximal connector. The housing distal open end is closed by a header that is movable between a closed position resting on the housing open end and an open position spaced there above. The header has a pair of side-by-side longitudinally extending openings. With the header in the open position, a practitioner holds the distal connector in one hand and with the other hand inserts the distal electrical contacts of one or two therapy delivery devices into the longitudinally extending openings.

Abstract: A device that is implantable in body tissue of a human or animal. The device is comprised of a header comprising at least one terminal adapted for removable connection to a lead and an open ended case closed by a plate to form a housing. The housing is comprised of a surrounding edge wall joined to a first side wall and a second side wall opposed to the first side wall. At least a first suture port extends through the edge wall and the second side wall but not the first side wall at an upper edge region of the housing. A second suture port may extend through the surrounding edge wall and the second side wall but not the first side wall in a similar manner. A third suture port may extend through the header. The three suture ports may define a triangular attachment configuration.