510(k) K122872 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Dio Medical Co., Ltd., Brea CA, US |
| Decision | Substantially Equivalent, Feb 28, 2013 |
| Received | Sep 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122872
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.