510(k) K142251 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
AVS AS PEEK Spacer
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Nov 19, 2014 |
| Received | Aug 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142251
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.