510(k) K120401 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ALAMO T
| Applicant | Alliance Partners, LLC, Avon Lake OH, US |
| Decision | Substantially Equivalent, Oct 5, 2012 |
| Received | Feb 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120401
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.