K253772
- 510(k) number
- K253772
- Device name
- Velocity Alpha MR High Speed Surgical Drill System
- Applicant
- Adeor Medical AG DE
- Product code
- HBB — Motor, Drill, Pneumatic
- Decision date
- 2026-03-06
- Date received
- 2025-11-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K253772.pdf
Official FDA record: K253772
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.