510(k) K082712 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
THEKEN SPINE VU EPOD AND VU LPOD SYSTEM
| Applicant | Theken Spine, LLC, Akron OH, US |
| Decision | Substantially Equivalent, Jan 2, 2009 |
| Received | Sep 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082712
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.