510(k) K133200 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
STALIF C(R)
| Applicant | Centinel Spine, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, May 8, 2014 |
| Received | Oct 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133200
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.