K254215
- 510(k) number
- K254215
- Device name
- Arthrex Beaming System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2026-05-08
- Date received
- 2025-12-29
- 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: K254215.pdf
Official FDA record: K254215
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.