FDA 510(k)

CAVUX 頸椎間置體-L SA 系統

K 號：K163474 · 2017-03-10

決定日期2017-03-10

產品代碼OVE

諮詢委員會或

決定相當於

器材摘要

CAVUX CervicalCage-L SA System 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 2017-03-10 under 510(k) number K163474. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CAVUX CervicalCage-L SA System?

CAVUX CervicalCage-L SA System is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K163474.

When did CAVUX CervicalCage-L SA System receive FDA 510(k) clearance?

CAVUX CervicalCage-L SA System received FDA 510(k) clearance on 2017-03-10, under 510(k) number K163474.

Who is the listed applicant for CAVUX CervicalCage-L SA System?

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 CervicalCage-L SA System?

The FDA product code for CAVUX CervicalCage-L SA System is OVE.

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。

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相關器械（代碼：OVE）

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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