510(k) K101363 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VU CPOD INTERVERTEBRAL BODU FUSION DEVICE
| Applicant | Musculoskeletal Clinical Regulatory Advisers, Washington DC, US |
| Decision | Substantially Equivalent, Dec 16, 2010 |
| Received | May 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101363
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.