Cortium
K-Number: K230614 · 2023-05-02
ApplicantUlrich Medical USA
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.
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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.