510(k) K082270 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM
| Applicant | Vertiflex, Inc., San Clamente CA, US |
| Decision | Substantially Equivalent, Sep 16, 2008 |
| Received | Aug 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082270
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.