510(k) K151496 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Latitude-C Cervical Interbody Spacer System
| Applicant | Degen Medical, Florence SC, US |
| Decision | Substantially Equivalent, Dec 15, 2015 |
| Received | Jun 3, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151496
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.