510(k) K123607 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OCTANE ELEVATE SPINAL IMPLANT SYSTEM
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Apr 25, 2014 |
| Received | Nov 21, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123607
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.