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FDA 510(k)

Vent Creativity Knee v1.0 (Hermes)

K-Number: K241961 · 2025-03-20

ApplicantVent Creativity
Decision Date2025-03-20
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Vent Creativity. The 510(k) number is K241961.

When was Vent Creativity Knee v1.0 (Hermes) approved by the FDA?

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

What company makes Vent Creativity Knee v1.0 (Hermes)?

Vent Creativity Knee v1.0 (Hermes) is manufactured by Vent Creativity.

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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