510(k) K212446 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NuVasive Anterior Cervical Plate Systems
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 3, 2021 |
| Received | Aug 5, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212446
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.