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FDA 510(k)

雙重醫療籠架系統

K 號：K172828 · 2018-02-01

申請人Double Medical Technology, Inc.
決定日期2018-02-01
產品代碼MAX
諮詢委員會或
決定相當於

器材摘要

Double Medical Cage System is the device name listed in this FDA 510(k) record. The listed applicant is Double Medical Technology, Inc.. It received FDA 510(k) clearance on 2018-02-01 under 510(k) number K172828. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Double Medical Cage System?

Double Medical Cage System is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Double Medical Technology, Inc.. The 510(k) number is K172828.

When did Double Medical Cage System receive FDA 510(k) clearance?

Double Medical Cage System received FDA 510(k) clearance on 2018-02-01, under 510(k) number K172828.

Who is the listed applicant for Double Medical Cage System?

The FDA 510(k) record lists Double Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Double Medical Cage System?

The FDA product code for Double Medical Cage System is MAX.

相關臨床試驗

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其他以 Double 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：MAX）

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

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