510(k) K213989 ยท HAW Neurological Stereotaxic Instrument
Cranial EM System
| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Sep 8, 2022 |
| Received | Dec 20, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213989
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.