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FDA 510(k)

Gemini Medical Cage System

K-Number: K242267 · 2024-10-08

ApplicantZheJiang Decans Medical Devices Co., Ltd.
Decision Date2024-10-08
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Gemini Medical Cage System is the device name listed in this FDA 510(k) record. The listed applicant is ZheJiang Decans Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2024-10-08 under 510(k) number K242267. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Gemini Medical Cage System?

Gemini Medical Cage System is a medical device that received FDA 510(k) clearance on 2024-10-08. The listed applicant is ZheJiang Decans Medical Devices Co., Ltd.. The 510(k) number is K242267.

When did Gemini Medical Cage System receive FDA 510(k) clearance?

Gemini Medical Cage System received FDA 510(k) clearance on 2024-10-08, under 510(k) number K242267.

Who is the listed applicant for Gemini Medical Cage System?

The FDA 510(k) record lists ZheJiang Decans Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Gemini Medical Cage System?

The FDA product code for Gemini Medical Cage System is MAX.

Other records listing ZheJiang Decans Medical Devices Co., Ltd. as applicant

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Related Devices (Code: MAX)

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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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