510(k) K203520 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Blustone Synergy Interbody Fusion System
| Applicant | Blustone Synergy, LLC, Pueblo CO, US |
| Decision | Substantially Equivalent, Apr 7, 2021 |
| Received | Dec 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203520
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.