510(k) K031657 ยท MRW System, Facet Screw Spinal Device
STRYKER SPINE OASYS BONE SCREW
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 22, 2003 |
| Received | May 28, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031657
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.