510(k) K150152 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
The Octane Straight Intervertebral Fusion Device, Ti Coated
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, May 11, 2015 |
| Received | Jan 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150152
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.