510(k) K233912 ยท HWC Screw, Fixation, Bone
ARIX Cannulated Screw System
| Applicant | Jeil Medical Corporation, Seoul, KR |
| Decision | Substantially Equivalent, Mar 11, 2024 |
| Received | Dec 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233912
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.