510(k) K233144 ยท HAW Neurological Stereotaxic Instrument
ClearPoint Bone Screw Fiducials
| Applicant | ClearPoint Neuro, Inc., Solana Beach CA, US |
| Decision | Substantially Equivalent, Jan 12, 2024 |
| Received | Sep 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233144
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.