510(k) K233703 ยท HAW Neurological Stereotaxic Instrument
Bone Anchor (NGS-BA-01)
| Applicant | ClearPoint Neuro, Inc., Solana Beach CA, US |
| Decision | Substantially Equivalent, Apr 26, 2024 |
| Received | Nov 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233703
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.