510(k) K223231 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Ti-Largo Cervical Interbody System
| Applicant | Flospine, Boca Raton FL, US |
| Decision | Substantially Equivalent, Feb 24, 2023 |
| Received | Oct 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223231
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.