510(k) K160418 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PERIMETER Interbody Fusion Device
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Mar 7, 2016 |
| Received | Feb 16, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K160418
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.