510(k) K121288 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FUSE CAGE
| Applicant | Advanced Medical Technologies AG, Nonnweiler-Braunshausen, DE |
| Decision | Substantially Equivalent, Jun 29, 2012 |
| Received | Apr 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121288
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.