510(k) K111983 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX
| Applicant | Zimmer Trabecular Metal Technology, Parsippany NJ, US |
| Decision | Substantially Equivalent, Nov 18, 2011 |
| Received | Jul 12, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111983
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.