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FDA 510(k)

Evolution® 全膝系統 - 運動學對齊儀器和技術

K 號:K243574 · 2025-02-18

決定日期2025-02-18
產品代碼JWH
諮詢委員會或
決定相當於

器材摘要

Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique is the device name listed in this FDA 510(k) record. The listed applicant is Microport Orthopedics, Inc.. It received FDA 510(k) clearance on 2025-02-18 under 510(k) number K243574. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique?

Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique is a medical device that received FDA 510(k) clearance on 2025-02-18. The listed applicant is Microport Orthopedics, Inc.. The 510(k) number is K243574.

When did Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique receive FDA 510(k) clearance?

Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique received FDA 510(k) clearance on 2025-02-18, under 510(k) number K243574.

Who is the listed applicant for Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique?

FDA 510(k) 記錄將 Microport Orthopedics, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique?

The FDA product code for Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and Technique is JWH.

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其他以 Microport Orthopedics, Inc. 為申請人之記錄

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相關器械(代碼:JWH)

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。

官方來源

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