510(k) K160715 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AccuLIF TL and PL Cage
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 8, 2016 |
| Received | Mar 15, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160715
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.