510(k) K200458 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tailored-C Cervical Interbody Fusion System
| Applicant | Bespoke Technologies, Winston-Salemn NC, US |
| Decision | Substantially Equivalent, Dec 28, 2020 |
| Received | Feb 25, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200458
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.