510(k) K222515 ยท MRW System, Facet Screw Spinal Device
FaSet Fixation System
| Applicant | Dio Medical Corporation, East Norriton PA, US |
| Decision | Substantially Equivalent, Oct 5, 2022 |
| Received | Aug 19, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222515
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.