K241961
- 510(k) number
- K241961
- Device name
- Vent Creativity Knee v1.0 (Hermes)
- Applicant
- Vent Creativity NY · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-03-20
- Date received
- 2024-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K241961.pdf
Official FDA record: K241961
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.