510(k) K243782 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
StimTrial Neuromodulation System
| Applicant | Bioventus, LLC, Durham NC, US |
| Decision | Substantially Equivalent, Jul 16, 2025 |
| Received | Dec 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243782
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.