510(k) K132584 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, Dec 4, 2013 |
| Received | Aug 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132584
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.