510(k) K121211 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
VU APOD INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Theken Spine, LLC, Medina OH, US |
| Decision | Substantially Equivalent, Jun 27, 2012 |
| Received | Apr 20, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121211
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.