510(k) K172480 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
icotec Interbody Cage System
| Applicant | Icotec AG, 9450 Altstaetten (Sg), CH |
| Decision | Substantially Equivalent, May 17, 2018 |
| Received | Aug 16, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172480
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.