510(k) K223719 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System
| Applicant | Aegis Spine, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jan 11, 2023 |
| Received | Dec 12, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223719
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.