510(k) K202309 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Epic Anterior Thoracolumbar Plate System, Gallery Laminoplasty Fixation System, Concero Facet Screw System, Alpine XC Adjustable Fusion System, Aspen MIS Fusion System, L-Plate MIS Fusion System
| Applicant | Zimmer Biomet Spine, Inc., Westminister CO, US |
| Decision | Substantially Equivalent, Oct 8, 2020 |
| Received | Aug 14, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202309
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.