510(k) K220951 ยท MRW System, Facet Screw Spinal Device
PMT Facet Fixation System (PMT FFS)
| Applicant | Providence Medical Technology, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Dec 9, 2022 |
| Received | Apr 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220951
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.