510(k) K083661 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVS TL PEEK SPACERS
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Feb 27, 2009 |
| Received | Dec 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083661
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.