510(k) K160924 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Amendia Interbody Fusion Devices
| Applicant | Amendia, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Nov 8, 2016 |
| Received | Apr 4, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160924
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.