510(k) K171489 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Acapella Cervical Spacer System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, Oct 23, 2017 |
| Received | May 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171489
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.