510(k) K100042 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM
| Applicant | Difusion Technologies, Austin TX, US |
| Decision | Substantially Equivalent, Oct 1, 2010 |
| Received | Jan 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100042
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.