510(k) K200482 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
StimRouter Neuromodulation System
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Mar 27, 2020 |
| Received | Feb 27, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K200482
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.