K252790
- 510(k) number
- K252790
- Device name
- Digital ClarusScope System and Digital NeuroPEN System
- Applicant
- Clarus Medical, LLC MN · US
- Product code
- HRX — Arthroscope
- Decision date
- 2026-05-26
- Date received
- 2025-09-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K252790.pdf
Official FDA record: K252790
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.