K252111
- 510(k) number
- K252111
- Device name
- Versius Surgical System (Versius Plus)
- Applicant
- Cmr Surgical Limited GB
- Product code
- SCV — Modular Electromechanical Surgical System
- Decision date
- 2025-12-16
- Date received
- 2025-07-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K252111.pdf
Official FDA record: K252111
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.