510(k) K100967 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
PERIMETER C SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Aug 5, 2011 |
| Received | Apr 8, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100967
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.