510(k) K093669 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SEC IBF CAGE
| Applicant | Innvotec Surgical, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Mar 18, 2010 |
| Received | Nov 27, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093669
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.