510(k) K143685 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Hedgehog Cervical Interbody Fusion Device
| Applicant | Vertera, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Sep 23, 2015 |
| Received | Dec 24, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143685
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.