Implantable Medical Device Connector System
An implantable medical stimulation device is provided including non-weld connections between one or more feed-through conductors and electrical contacts of a connector block for the device. The device can be configured for implantation into a pelvic region of a patient to provide muscle and/or nerve stimulation that is used to control and/or treat a pelvic condition of the patient, such as pelvic pain, urinary incontinence, fecal incontinence, erectile dysfunction or other pelvic conditions. The non-weld connections serve to simplify connectivity by providing an insertable wedge-like member, or a crimping member, adapted to facilitate selective electrical connectivity.
1 . An implantable stimulator device, comprising:
a control unit including;
electronic circuitry;
a feed-through conductor operably coupleable to the electronic circuitry and extendable outside of the control unit;
a header including a connector block having an electrical contact, and an opening adjacent the electrical contact configured to receive an end of the feed-through conductor;
an access port to the opening adjacent the electrical contact; and
a member insertable through the access port, between an interior wall of the opening and the end of the feed-through conductor, to secure the conductor in electrical communication with the electrical contact.
2 . The device of claim 1 , wherein the member is generally tapered to define a wedge member.
3 . The device of claim 1 , wherein at least one of the member or the end of the feed-through conductor is generally deformable.
4 . The device of claim 1 , wherein the member is electrically conductive.
5 . The device of claim 1 , wherein a distal end of the feed-through conductor includes an electrode adapted for stimulating tissue.
6 . The device of claim 1 , further including means for sealing off at least a portion of the access port to prevent fluid from entering the access port.
7 . The device of claim 1 , wherein the feed-through conductor further includes a lead body extending outside of the control unit.
8 . The device of claim 1 , wherein the control unit is adapted for implantation under the skin of the abdomen or genital region of a patient.
9 . An implantable stimulator device, comprising:
a device housing including electronics;
a feed-through conductor operably coupleable to the electronics and extendable outside of the device housing; and
a header including a connector block having an electrical contact, and an opening adjacent the electrical contact configured to receive an end of the feed-through conductor; and
a crimping member adjacent the electrical contact and adapted to secure the end of the conductor in electrical communication with the electrical contact.
10 . The device of claim 9 , further including a crimping tool adapted to crimp the crimping member.
11 . The device of claim 9 , wherein the crimping member is a deformable tube member.
12 . The device of claim 9 , wherein the crimping member is electrically conductive.
13 . The device of claim 9 , wherein a distal end of the feed-through conductor includes an electrode adapted for stimulating tissue.
14 . The device of claim 9 , further including means for sealing off at least a portion of the opening to prevent fluid from entering the opening.
15 . The device of claim 9 , wherein the feed-through conductor further includes a lead body extending outside of the control unit.
16 . The device of claim 9 , wherein the device housing is adapted for implantation under the skin of the abdomen or genital region of a patient.
17 . A method of providing electrical stimulation to a patient, comprising:
providing an implantable stimulator device adapted for implantation in a patient, the implantable stimulator device including a control unit and a header, the control unit housing electronics, and the header including a connector block having an electrical contact and an opening adjacent the electrical contact, with a feed-through conductor operably and electrically coupleable to the electronics;
inserting an end of the feed-through conductor into the opening;
manipulating a member to provide electrical communication between the feed-through conductor and the electrical contact; and
implanting the stimulator device in the pelvic region of the patient.
18 . The method of claim 17 , wherein the member is a tapered wedge member.
19 . The method of claim 17 , wherein the member is a crimping member.
20 . The method of claim 17 , wherein the member is electrically conductive.