510(k) K100865 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVA NAVIGATOR PEEK SPACERS, MODEL 48392XXX, 48393XXX
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 11, 2010 |
| Received | Mar 29, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100865
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.