510(k) K101051 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AVS A-LAT PEEK SPACERS, MODELS 48750XXX, 48751XXX, 48752XXX, 48753XXX
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Aug 12, 2010 |
| Received | Apr 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101051
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.