GS醫療 AnyPlus PEEK 金屬網架系統
K 號：K200592 · 2020-08-10
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器材摘要
GS Medical AnyPlus PEEK Cage System is the device name listed in this FDA 510(k) record. The listed applicant is GS Medical Co., Ltd.. It received FDA 510(k) clearance on 2020-08-10 under 510(k) number K200592. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
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. The listed applicant is GS Medical Co., Ltd.. The 510(k) number is K200592.
When did GS Medical AnyPlus PEEK Cage System receive FDA 510(k) clearance?
GS Medical AnyPlus PEEK Cage System received FDA 510(k) clearance on 2020-08-10, under 510(k) number K200592.
Who is the listed applicant for GS Medical AnyPlus PEEK Cage System?
FDA 510(k)記錄將GS Medical Co., Ltd.列為申請人。這本身並不足以確立設備製造商。
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.
相關臨床試驗
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其他以 GS Medical Co., Ltd. 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
相關器械（代碼：ODP）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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