510(k) K234092 ยท GWF Stimulator, Electrical, Evoked Response
SafeOp 3: Neural Informatix Systeem
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Apr 19, 2024 |
| Received | Dec 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234092
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.