510(k) K123969 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
XIPHOS
| Applicant | Difusion Technologies, Chesterland OH, US |
| Decision | Substantially Equivalent, Feb 7, 2013 |
| Received | Dec 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123969
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.