510(k) K130948 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
C-FUSE CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
| Applicant | Southern Spine, LLC, Alpharetta GA, US |
| Decision | Substantially Equivalent, Aug 14, 2013 |
| Received | Apr 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130948
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.