K233912
- 510(k) number
- K233912
- Device name
- ARIX Cannulated Screw System
- Applicant
- Jeil Medical Corporation KR
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2024-03-11
- Date received
- 2023-12-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233912.pdf
Official FDA record: K233912
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.