510(k) K202575 ยท HAW Neurological Stereotaxic Instrument
ClearPoint Array System
| Applicant | ClearPoint Neuro, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 22, 2021 |
| Received | Sep 4, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202575
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.