510(k) K243657 ยท HAW Neurological Stereotaxic Instrument
ClearPoint System (Software Version 3.0)
| Applicant | ClearPoint Neuro, Inc., Solana Beach CA, US |
| Decision | Substantially Equivalent, Jan 24, 2025 |
| Received | Nov 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243657
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.