510(k) K151755 ยท NKG Posterior Cervical Screw System
OASYS(r) System
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 9, 2015 |
| Received | Jun 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151755
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.