卡博潔明導航儀器
K 號：K201251 · 2020-08-05
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器材摘要
CarboClear Navigated Instruments is the device name listed in this FDA 510(k) record. The listed applicant is CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2020-08-05 under 510(k) number K201251. 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 CarboClear Navigated Instruments?
CarboClear Navigated Instruments is a medical device that received FDA 510(k) clearance on 2020-08-05. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K201251.
When did CarboClear Navigated Instruments receive FDA 510(k) clearance?
CarboClear Navigated Instruments received FDA 510(k) clearance on 2020-08-05, under 510(k) number K201251.
Who is the listed applicant for CarboClear Navigated Instruments?
The FDA 510(k) record lists CarboFix Orthopedics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CarboClear Navigated Instruments?
The FDA product code for CarboClear Navigated Instruments is OLO.
相關臨床試驗
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其他以 CarboFix Orthopedics , 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：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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