510(k) K111675 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
VU C*POD INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Theken Spine, LLC, Medina OH, US |
| Decision | Substantially Equivalent, Aug 2, 2011 |
| Received | Jun 15, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111675
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.