GS Medical AnyPlus PEEK Cage System
K-Number: K200592 · 2020-08-10
ApplicantGS Medical Co., Ltd.
Decision Date2020-08-10
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
GS Medical AnyPlus PEEK Cage System is a medical device manufactured by GS Medical Co., Ltd.. It received FDA 510(k) clearance on 2020-08-10 under approval number K200592. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the GS Medical AnyPlus PEEK Cage System?
GS Medical AnyPlus PEEK Cage System is a medical device that received FDA 510(k) clearance on 2020-08-10. It is manufactured by GS Medical Co., Ltd.. The 510(k) number is K200592.
When was GS Medical AnyPlus PEEK Cage System approved by the FDA?
GS Medical AnyPlus PEEK Cage System received FDA 510(k) clearance on 2020-08-10, under approval number K200592.
What company makes GS Medical AnyPlus PEEK Cage System?
GS Medical AnyPlus PEEK Cage System is manufactured by GS Medical Co., Ltd..
What is the FDA product code for GS Medical AnyPlus PEEK Cage System?
The FDA product code for GS Medical AnyPlus PEEK Cage System is ODP.
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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.