510(k) K150847 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Foundation Interbody Devices
| Applicant | Corelink, LLC, St.Louis MO, US |
| Decision | Substantially Equivalent, Aug 13, 2015 |
| Received | Mar 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150847
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.