510(k) K140303 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ALAMO T
| Applicant | Alliance Partners, LLC, Memphis TN, US |
| Decision | Substantially Equivalent, Apr 21, 2014 |
| Received | Feb 6, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140303
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.