510(k) K110543 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CRESCENT (R) SPINAL SYSTEM TITANIUM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Aug 9, 2011 |
| Received | Feb 25, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110543
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.