510(k) K130434 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
OCTANE STRAIGHT, OCTANE STRAIGHT - LORDOTIC, OCTANE STRAIGHT I/R, OCTANE STRAIGHT I/R - LORDOTIC
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, May 1, 2013 |
| Received | Feb 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130434
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.