510(k) K211965 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
StimRouter Neuromodulation System
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Feb 23, 2022 |
| Received | Jun 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211965
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.