CAVUX™ 頸椎籠
K 號：K161642 · 2016-10-07
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器材摘要
CAVUX™ Cervical Cage 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 2016-10-07 under 510(k) number K161642. 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 CAVUX™ Cervical Cage?
CAVUX™ Cervical Cage is a medical device that received FDA 510(k) clearance on 2016-10-07. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K161642.
When did CAVUX™ Cervical Cage receive FDA 510(k) clearance?
CAVUX™ Cervical Cage received FDA 510(k) clearance on 2016-10-07, under 510(k) number K161642.
Who is the listed applicant for CAVUX™ Cervical Cage?
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 CAVUX™ Cervical Cage?
The FDA product code for CAVUX™ Cervical Cage is ODP.
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：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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