510(k) K111123 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VARILIFT CERVICAL INTERBODY FUSION SYSTEM
| Applicant | Wenzel Spine, Round Rock TX, US |
| Decision | Substantially Equivalent, Dec 8, 2011 |
| Received | Apr 21, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111123
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.