FDA 510(k)

LOQTEQ 腳板電極 2.5

K 號：K182785 · 2019-06-19

決定日期2019-06-19

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

LOQTEQ VA Foot Plates 2.5 is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2019-06-19 under 510(k) number K182785. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LOQTEQ VA Foot Plates 2.5?

LOQTEQ VA Foot Plates 2.5 is a medical device that received FDA 510(k) clearance on 2019-06-19. The listed applicant is Aap Implantate AG. The 510(k) number is K182785.

When did LOQTEQ VA Foot Plates 2.5 receive FDA 510(k) clearance?

LOQTEQ VA Foot Plates 2.5 received FDA 510(k) clearance on 2019-06-19, under 510(k) number K182785.

Who is the listed applicant for LOQTEQ VA Foot Plates 2.5?

The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOQTEQ VA Foot Plates 2.5?

The FDA product code for LOQTEQ VA Foot Plates 2.5 is HRS.

其他以 Aap Implantate AG 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：HRS）

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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