510(k) K160600 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
Freedom Spinal Cord Stimulator System
| Applicant | Stimwave Technologies Incorporated, Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Aug 26, 2016 |
| Received | Mar 2, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160600
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.