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FDA 510(k)

Cortium™

K-Number: K230614 · 2023-05-02

Decision Date2023-05-02
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cortium™ is a medical device manufactured by Ulrich Medical USA. It received FDA 510(k) clearance on 2023-05-02 under approval number K230614. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cortium™?

Cortium™ is a medical device that received FDA 510(k) clearance on 2023-05-02. It is manufactured by Ulrich Medical USA. The 510(k) number is K230614.

When was Cortium™ approved by the FDA?

Cortium™ received FDA 510(k) clearance on 2023-05-02, under approval number K230614.

What company makes Cortium™?

Cortium™ is manufactured by Ulrich Medical USA.

What is the FDA product code for Cortium™?

The FDA product code for Cortium™ is NKG.

Other Devices by Ulrich Medical USA

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Related Devices (Code: NKG)

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.