510(k) K151310 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Amendia Interbody Fusion Devices
| Applicant | Amendia, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Jan 6, 2016 |
| Received | May 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151310
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.