510(k) K132029 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
VAULT-C INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Spinal USA, Colorado Springs CO, US |
| Decision | Substantially Equivalent, Nov 25, 2013 |
| Received | Jul 1, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132029
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.