StimRouter Registry Clinical Protocol

StimRouter Registry Clinical Protocol

This Registry study will prospectively evaluate the long-term effectiveness, safety, and tolerability of the StimRouter Neuromodulation System, along with evaluating the technical performance of StimRouter, surgical outcomes, health-related quality of life, concomitant medical use, and subject's impression of improvement.

No pharmaceutical medication involved
Patients and healthy individuals accepted

Device - StimRouter Neuromodulation System

An implantable neuromodulation device that treats chronic peripheral nerve pain.

A Prospective, Open-label, Long-term, Multi-center, Registry to Assess the Safety and Efficacy of the Bioness StimRouter Neuromodulation System in Subjects With Chronic Pain of Peripheral Nerve Origin