510(k) K212937 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Dakota ALIF Plate System
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Nov 4, 2021 |
| Received | Sep 15, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212937
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.