510(k) K242260 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 15, 2024 |
| Received | Jul 31, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242260
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.