510(k) K203253 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
NuVasive ACP System
| Applicant | Nu Vasive, Incorporated, San Diego CA, US |
| Decision | Substantially Equivalent, Dec 3, 2020 |
| Received | Nov 4, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203253
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.