510(k) K082309 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CAMBRIA
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Apr 9, 2009 |
| Received | Aug 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082309
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.