510(k) K073470 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVS PL PEEK SPACERS, MODELS 48351XXX AND 48353XXX
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Mar 6, 2008 |
| Received | Dec 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073470
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.