FDA 510(k)

Arthrosurface WristMotion 總腕關節置换系統

K 號：K200718 · 2020-10-15

決定日期2020-10-15

產品代碼JWJ

諮詢委員會或

決定相當於

器材摘要

Arthrosurface WristMotion Total Wrist Arthroplasty System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrosurface, Inc.. It received FDA 510(k) clearance on 2020-10-15 under 510(k) number K200718. The device is classified under product code JWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Arthrosurface WristMotion Total Wrist Arthroplasty System?

Arthrosurface WristMotion Total Wrist Arthroplasty System is a medical device that received FDA 510(k) clearance on 2020-10-15. The listed applicant is Arthrosurface, Inc.. The 510(k) number is K200718.

When did Arthrosurface WristMotion Total Wrist Arthroplasty System receive FDA 510(k) clearance?

Arthrosurface WristMotion Total Wrist Arthroplasty System received FDA 510(k) clearance on 2020-10-15, under 510(k) number K200718.

Who is the listed applicant for Arthrosurface WristMotion Total Wrist Arthroplasty System?

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

What is the FDA product code for Arthrosurface WristMotion Total Wrist Arthroplasty System?

The FDA product code for Arthrosurface WristMotion Total Wrist Arthroplasty System is JWJ.

其他以 Arthrosurface, 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：JWJ）

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。

K243381全腕關節置換系統 (TWA)Skeletal Dynamics, Inc.K233574全腕關節置換系統 (TWA)Skeletal Dynamics K233674自由手腕關節成形系統Ascension Orthopedics, Inc.K191525KinematX 全腕關節置換系統Extremity Medical, LLC

官方來源

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