510(k) K122850 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES
| Applicant | Meditech Advisors, LLC, Ashland MA, US |
| Decision | Substantially Equivalent, Mar 28, 2013 |
| Received | Sep 18, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122850
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.