510(k) K120603 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VARILIFT -C
| Applicant | Wenzel Spine, Austin TX, US |
| Decision | Substantially Equivalent, Jan 29, 2013 |
| Received | Feb 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120603
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.