510(k) K162496 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Foundation 3D Interbody
| Applicant | Corelink, LLC, St. Louis MO, US |
| Decision | Substantially Equivalent, May 4, 2017 |
| Received | Sep 7, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162496
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.