FDA 510(k)

Vent Creativity Knee v1.0 (Hermes)

Número K: K241961 · 2025-03-20

Data da decisão2025-03-20

Código do produtoQIH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vent Creativity Knee v1.0 (Hermes) is the device name listed in this FDA 510(k) record. The listed applicant is Vent Creativity. It received FDA 510(k) clearance on 2025-03-20 under 510(k) number K241961. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vent Creativity Knee v1.0 (Hermes)?

Vent Creativity Knee v1.0 (Hermes) is a medical device that received FDA 510(k) clearance on 2025-03-20. The listed applicant is Vent Creativity. The 510(k) number is K241961.

When did Vent Creativity Knee v1.0 (Hermes) receive FDA 510(k) clearance?

Vent Creativity Knee v1.0 (Hermes) received FDA 510(k) clearance on 2025-03-20, under 510(k) number K241961.

Who is the listed applicant for Vent Creativity Knee v1.0 (Hermes)?

The FDA 510(k) record lists Vent Creativity as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vent Creativity Knee v1.0 (Hermes)?

The FDA product code for Vent Creativity Knee v1.0 (Hermes) is QIH.

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