510(k) K120486 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
AVS AS PEEK SPACER
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 20, 2012 |
| Received | Feb 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120486
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.