510(k) K152532 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
AERO -C Cervical Cage System
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Dec 18, 2015 |
| Received | Sep 3, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152532
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.