510(k) K223288 ยท HAW Neurological Stereotaxic Instrument
Cranial Navigation, Navigation Software Cranial, Navigation Software Craniofacial, Cranial EM System, Automatic Registration iMRI
| Applicant | Brainlab AG, Munich, DE |
| Decision | Substantially Equivalent, Jul 21, 2023 |
| Received | Oct 25, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223288
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.