510(k) K173099 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Fortis and Hana Anterior Cervical Plate System
| Applicant | Huvexel Co. , Ltd., Seongnam-Si, KR |
| Decision | Substantially Equivalent, Nov 30, 2017 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173099
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.