Vent Creativity Knee v1.0 (Hermes)— 510(k) K241961

Name: FDA 510(k) clearance K241961
Creator: U.S. Food and Drug Administration
Published: 2025-03-20

Substantially Equivalent

Vent Creativity

FDA 510(k) clearance K241961 for Vent Creativity Knee v1.0 (Hermes), Substantially Equivalent on 2025-03-20. Applicant: Vent Creativity. Device class: 2.

Clearance details

Applicant: Vent Creativity
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2024-07-03
Decision date: 2025-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.