510(k) K210521 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
DEXA-C Cervical Interbody System
| Applicant | Aurora Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 2, 2021 |
| Received | Feb 23, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210521
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.