510(k) K100214 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Jun 25, 2010 |
| Received | Jan 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100214
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.