510(k) K160222 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
OIC Cervical PEEK Spacer
| Applicant | The Orthopaedic Implant Company, Reno NV, US |
| Decision | Substantially Equivalent, Dec 7, 2016 |
| Received | Jan 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160222
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.