510(k) K230840 ยท MRW System, Facet Screw Spinal Device
PMT Facet Fixation System, Lumbar (PMT FFS-LX)
| Applicant | Providence Medical Technology, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Dec 19, 2023 |
| Received | Mar 27, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230840
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.