510(k) K130863 ยท MRW System, Facet Screw Spinal Device
FACET SCREW SYSTEM
| Applicant | Spinal USA, Philedelphia PA, US |
| Decision | Substantially Equivalent, Aug 9, 2013 |
| Received | Mar 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130863
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.