510(k) K220324 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AccuFit Lateral 2-Hole Plate
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Mar 16, 2022 |
| Received | Feb 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220324
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.