510(k) K253190 ยท MRW System, Facet Screw Spinal Device
CORUS-LX Implant
| Applicant | Providence Medical Technology, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Nov 20, 2025 |
| Received | Sep 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253190
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.