510(k) K111965 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VUSION(R) OS
| Applicant | Ortho Development, Draper UT, US |
| Decision | Substantially Equivalent, Oct 25, 2011 |
| Received | Jul 11, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111965
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.