510(k) K173030 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Vertera Spine Cohere Cervical Interbody Fusion Device
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 21, 2017 |
| Received | Sep 28, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173030
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.