FDA 510(k)

EZ-TRAX 購姆 G7 骨盆系統 / Taperloc 完整股骨系統包裝設備

K 號：K213209 · 2021-12-28

決定日期2021-12-28

產品代碼KCT

諮詢委員會醫療設備規範文本翻譯如下： HO 注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。

決定相當於

器材摘要

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device is the device name listed in this FDA 510(k) record. The listed applicant is K1 Medical, LLC. It received FDA 510(k) clearance on 2021-12-28 under 510(k) number K213209. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device?

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device is a medical device that received FDA 510(k) clearance on 2021-12-28. The listed applicant is K1 Medical, LLC. The 510(k) number is K213209.

When did EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device receive FDA 510(k) clearance?

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device received FDA 510(k) clearance on 2021-12-28, under 510(k) number K213209.

Who is the listed applicant for EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device?

The FDA 510(k) record lists K1 Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device?

The FDA product code for EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device is KCT.

其他以 K1 Medical, LLC 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：KCT）

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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