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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 the device name listed in this FDA 510(k) record. The listed applicant is Ulrich Medical USA. It received FDA 510(k) clearance on 2023-05-02 under 510(k) 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. The listed applicant is Ulrich Medical USA. The 510(k) number is K230614.

When did Cortium™ receive FDA 510(k) clearance?

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

Who is the listed applicant for Cortium™?

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

What is the FDA product code for Cortium™?

The FDA product code for Cortium™ is NKG.

Other records listing Ulrich Medical USA as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: NKG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.