510(k) K251885 ยท MRW System, Facet Screw Spinal Device
CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
| Applicant | Providence Medical Technology, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Jul 10, 2025 |
| Received | Jun 20, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251885
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.