360CAS 開關節
K 號：K242009 · 2024-08-08
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器材摘要
360CAS Knee is the device name listed in this FDA 510(k) record. The listed applicant is Kico Knee Innovation Company Pty, Ltd.. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K242009. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the 360CAS Knee?
360CAS Knee is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is Kico Knee Innovation Company Pty, Ltd.. The 510(k) number is K242009.
When did 360CAS Knee receive FDA 510(k) clearance?
360CAS Knee received FDA 510(k) clearance on 2024-08-08, under 510(k) number K242009.
Who is the listed applicant for 360CAS Knee?
The FDA 510(k) record lists Kico Knee Innovation Company Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 360CAS Knee?
The FDA product code for 360CAS Knee is OLO.
其他以 Kico Knee Innovation Company Pty, Ltd. 為申請人之記錄
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相關器械（代碼：OLO）
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。
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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