510(k) K232102 ยท HAW Neurological Stereotaxic Instrument
ClearPoint Array System (Version 1.2)
| Applicant | ClearPoint Neuro, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 15, 2023 |
| Received | Jul 14, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232102
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.