K253713
- 510(k) number
- K253713
- Device name
- Arthrex Variable Angle (VA) Proximal Tibia Plating System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2026-01-21
- Date received
- 2025-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K253713.pdf
Official FDA record: K253713
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.