510(k) K100945 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FUSE PLIF CAFE
| Applicant | Advanced Medical Technologies AG, Round Rock TX, US |
| Decision | Substantially Equivalent, Feb 9, 2011 |
| Received | Apr 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100945
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.