510(k) K240423 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TDM Anterior Cervical Plate System
| Applicant | Tdm Co., Ltd., Gwangju, KR |
| Decision | Substantially Equivalent, Apr 8, 2024 |
| Received | Feb 13, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240423
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.