510(k) K171496 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tritanium C Anterior Cervical Cage
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Sep 6, 2017 |
| Received | May 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171496
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.