510(k) K230639 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Align Cervical Interbody Fusion System
| Applicant | Acuity Surgical Devices, LLC, Irving TX, US |
| Decision | Substantially Equivalent, Dec 1, 2023 |
| Received | Mar 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230639
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.