510(k) K202972 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Anterior Cervical Plate System
| Applicant | Nutech Spine and Biologics, Birmingham AL, US |
| Decision | Substantially Equivalent, Nov 24, 2020 |
| Received | Sep 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202972
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.