FDA 510(k)

LINK MobileLink® 髋臼杯系統 - 兩用性內襯片，以及殼/內置式適配器

K 號：K200607 · 2021-05-28

決定日期2021-05-28

產品代碼LPH

諮詢委員會或

決定相當於

器材摘要

LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 2021-05-28 under 510(k) number K200607. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters?

LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters is a medical device that received FDA 510(k) clearance on 2021-05-28. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K200607.

When did LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters receive FDA 510(k) clearance?

LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters received FDA 510(k) clearance on 2021-05-28, under 510(k) number K200607.

Who is the listed applicant for LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters?

The FDA product code for LINK MobileLink® Acetabular Cup System - Dual Mobility Liners, and Shell/Insert Adapters is LPH.

其他以 Waldemar Link GmbH & Co. KG 為申請人之記錄

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相關器械（代碼：LPH）

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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