CORUS™導航系統-GN
K 號：K261665 · 2026-06-18
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器材摘要
CORUS™ Navigation System-GN is the device name listed in this FDA 510(k) record. The listed applicant is Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K261665. 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 CORUS™ Navigation System-GN?
CORUS™ Navigation System-GN is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K261665.
When did CORUS™ Navigation System-GN receive FDA 510(k) clearance?
CORUS™ Navigation System-GN received FDA 510(k) clearance on 2026-06-18, under 510(k) number K261665.
Who is the listed applicant for CORUS™ Navigation System-GN?
The FDA 510(k) record lists Providence Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORUS™ Navigation System-GN?
The FDA product code for CORUS™ Navigation System-GN is OLO.
相關臨床試驗
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其他以 Providence Medical Technology, Inc. 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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