K252733
- 510(k) number
- K252733
- Device name
- ATLAS Expandable Osteotomy Wedge System
- Applicant
- MiRus, LLC GA · US
- Product code
- PLF — Bone Wedge
- Decision date
- 2026-02-19
- Date received
- 2025-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K252733.pdf
Official FDA record: K252733
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.