510(k) K122313 ยท JEY Plate, Bone
STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM
| Applicant | Stryker, Portage MI, US |
| Decision | Substantially Equivalent, Oct 31, 2012 |
| Received | Aug 1, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122313
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.