Resorbable anchor arrangements for implantable devices and methods of making and using

1. A stimulation system comprising:

a device body comprising

a lead having a distal portion and a proximal portion, the lead comprising, at least one terminal disposed on the proximal portion of the lead, and at least one conductor extending along the lead from the distal portion of the lead to the at least one terminal; and

at least one anchoring unit disposed at the distal portion of the lead such that the at least one anchoring unit is entirely disposed distal to the lead, the at least one anchoring unit configured and arranged for anchoring the distal portion of the lead in a patient upon implantation so that the at least one anchoring unit at least partially surrounds at least one nerve of a patient, the anchoring unit being cuff-shaped and defining a slit extending along a length of the anchoring unit that is configured and arranged to enable the at least one nerve to pass through the slit as the anchoring unit is being coupled to the at least one nerve, the anchoring unit comprising at least one electrode coupled to the at least one conductor and a resorbable material that resorbs into the patient over a period of time after implantation, the resorption at least partially releasing the at least one electrode from the anchoring unit while the device body is implanted in the patient, the at least one anchoring unit is configured and arranged such that the period of time of resorption is sufficient to allow tissue ingrowth around the at least one electrode to anchor the at least one electrode prior to release of the at least one electrode due to at least a partial resorption of the anchoring unit.

2. The stimulation system of claim 1 , wherein the at least one electrode is disposed on the at least one anchoring unit.

3. The stimulation system of claim 1 , wherein the anchoring unit is formed integrally with the device body.

4. A method of implanting the stimulation system of claim 1 , the method comprising:

implanting the device body of the stimulation system into a patient; and

coupling the anchoring unit of the stimulation system to at least one nerve of the patient so that the anchoring unit at least partially surrounds the at least one nerve of the patient, the anchoring unit being coupled to the device body to allow fixation of the device body to the at least one nerve.

5. The method of claim 4 , further comprising enhancing tissue growth around the at least one electrode.

6. The method of claim 4 , further comprising removing the device body after enough of the resorbable material is resorbed by the patient to at least partially release the at least one electrode from the anchoring unit.

7. The method of claim 4 , wherein the resorption of the anchoring unit fully releases at least one of the electrodes from the anchoring unit.

8. The method of claim 4 , wherein the at least one electrode is disposed on the at least one anchoring unit.

9. The stimulation system of claim 1 , wherein the resorption of the anchoring unit fully releases at least one of the electrodes from the anchoring unit.

10. The stimulation system of claim 1 , wherein the at least one conductor extends along at least a portion of the at least one anchoring unit in a direction that is parallel to the slit extending along the length of the at least one anchoring unit.

11. The stimulation system of claim 1 , wherein the device body is configured and arranged for explantation from the patient after the resorbable material is resorbed by the patient.

12. The stimulation system of claim 1 , wherein the device body further comprises an implantable pulse generator coupled to the proximal portion of the lead, wherein the implantable pulse generator provides electrical pulses along the at least one conductor to the at least one electrode.

13. The stimulation system of claim 12 , wherein the implantable pulse generator is configured and arranged for implantation at a location that is remote from the at least one anchoring unit.

14. The stimulation system of claim 12 , wherein the at least one terminal of the lead is configured and arranged for insertion into the implantable pulse generator.