510(k) K170844 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Gemini-C Hybrid Cervical Interbody System
| Applicant | Osseus Fusion Systems, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Jul 3, 2017 |
| Received | Mar 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170844
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.