FDA 510(k)

MobileLink 骨盆杯系統 - 線路擴展（多個）

K 號：K241636 · 2024-11-08

決定日期2024-11-08

產品代碼LPH

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器材摘要

MobileLink Acetabular Cup System - Line Extension (Multiple) 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 2024-11-08 under 510(k) number K241636. 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 MobileLink Acetabular Cup System - Line Extension (Multiple)?

MobileLink Acetabular Cup System - Line Extension (Multiple) is a medical device that received FDA 510(k) clearance on 2024-11-08. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K241636.

When did MobileLink Acetabular Cup System - Line Extension (Multiple) receive FDA 510(k) clearance?

MobileLink Acetabular Cup System - Line Extension (Multiple) received FDA 510(k) clearance on 2024-11-08, under 510(k) number K241636.

Who is the listed applicant for MobileLink Acetabular Cup System - Line Extension (Multiple)?

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 MobileLink Acetabular Cup System - Line Extension (Multiple)?

The FDA product code for MobileLink Acetabular Cup System - Line Extension (Multiple) 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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