510(k) K113642 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PERIMETER INTERBODY FUSION DEVICE
| Applicant | Medtronic Sofamor Danek USA, Memphis TN, US |
| Decision | Substantially Equivalent, Feb 6, 2012 |
| Received | Dec 12, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113642
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.