510(k) K080758 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVS PL PEEK SPACERS, MODELS 48351 AND 48353
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Mar 27, 2008 |
| Received | Mar 18, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080758
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.