Gemini Medical Cage System
K-Number: K242267 · 2024-10-08
Decision Date2024-10-08
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Gemini Medical Cage System is a medical device manufactured by ZheJiang Decans Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2024-10-08 under approval 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. It is manufactured by ZheJiang Decans Medical Devices Co., Ltd.. The 510(k) number is K242267.
When was Gemini Medical Cage System approved by the FDA?
Gemini Medical Cage System received FDA 510(k) clearance on 2024-10-08, under approval number K242267.
What company makes Gemini Medical Cage System?
Gemini Medical Cage System is manufactured by ZheJiang Decans Medical Devices Co., Ltd..
What is the FDA product code for Gemini Medical Cage System?
The FDA product code for Gemini Medical Cage System is MAX.
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Other Devices by ZheJiang Decans Medical Devices Co., Ltd.
K242195Gemini Cervical Fusion Cage System
K243665Crius PEEK Suture Anchor System (Thread-Fix Anchor); Crius PEEK Suture Anchor System (Thread-Fix Ultra Anchor); Crius PEEK Suture Anchor System (Helicoil Anchor); Crius PEEK Suture Anchor System (Pile Anchor)
K252776ARIES Anterior Cervical Plate Systems
K252542LEO Spinal System
K253213SAGI Cervical Cage System
K252774Uni-C Cervical Cage System
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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.