510(k) K152622 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Alta ACDF System
| Applicant | Biomet Spine, Broomfield CO, US |
| Decision | Substantially Equivalent, Jul 8, 2016 |
| Received | Sep 14, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152622
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.