510(k) K220513 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
NITRO Interbody Fusion Cage System Family
| Applicant | Ctl Medical Corporation, Addison TX, US |
| Decision | Substantially Equivalent, Apr 25, 2023 |
| Received | Feb 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220513
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.