510(k) K231103 ยท HAW Neurological Stereotaxic Instrument
ROSA ONE Brain Application
| Applicant | Medtech S.A.S, Mauguio, FR |
| Decision | Substantially Equivalent, Jul 20, 2023 |
| Received | Apr 19, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231103
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.