510(k) K121333 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
WAVE D CAGE
| Applicant | Advanced Medical Technologies AG, Round Rock TX, US |
| Decision | Substantially Equivalent, Jun 29, 2012 |
| Received | May 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121333
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.