510(k) K162262 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Tritanium® PL Cage
| Applicant | Stryker, Allendale NJ, US |
| Decision | Substantially Equivalent, Nov 9, 2016 |
| Received | Aug 11, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162262
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.