510(k) K112444 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ANATOMIC PEEK CERVICAL FUSION SYSTEM
| Applicant | Medtronic Sofamor Danck USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Nov 15, 2011 |
| Received | Aug 24, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112444
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.