510(k) K142079 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
STALIF CTI, STALIF C
| Applicant | Centinel Spine, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 24, 2014 |
| Received | Jul 31, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142079
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.