510(k) K203251 ยท HAW Neurological Stereotaxic Instrument
SOLOPASS System
| Applicant | Intravent Medical Partners, LP, Hershey PA, US |
| Decision | Substantially Equivalent, Aug 27, 2021 |
| Received | Nov 4, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203251
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.