510(k) K221303 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Neuspera Nuity System
| Applicant | Neuspera Medical, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Apr 11, 2023 |
| Received | May 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221303
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.