510(k) K153720 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ENZA Zero-Profile Anterior Interbody Fusion
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, May 3, 2016 |
| Received | Dec 28, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153720
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.