510(k) K192208 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CORNICE Cervical Spacer System
| Applicant | Legend Spine Technologies, Bethlehem PA, US |
| Decision | Substantially Equivalent, Oct 9, 2019 |
| Received | Aug 14, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192208
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.