510(k) K172212 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Jan 9, 2018 |
| Received | Jul 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172212
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.