510(k) K101310 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
VU APOD INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Theken Spine, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Sep 2, 2010 |
| Received | May 11, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101310
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.