510(k) K230026 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SQUALE
| Applicant | Implanet, S.A., Martillac, FR |
| Decision | Substantially Equivalent, Mar 28, 2023 |
| Received | Jan 4, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230026
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.