FDA 510(k)

Klassic膝關節系統 - 改良式胫骨基板

K 號：K243991 · 2025-03-24

決定日期2025-03-24

產品代碼JWH

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決定相當於

器材摘要

Klassic Knee System - Revision Tibial Baseplate is the device name listed in this FDA 510(k) record. The listed applicant is Total Joint Othopedics, Inc.. It received FDA 510(k) clearance on 2025-03-24 under 510(k) number K243991. 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 Klassic Knee System - Revision Tibial Baseplate?

Klassic Knee System - Revision Tibial Baseplate is a medical device that received FDA 510(k) clearance on 2025-03-24. The listed applicant is Total Joint Othopedics, Inc.. The 510(k) number is K243991.

When did Klassic Knee System - Revision Tibial Baseplate receive FDA 510(k) clearance?

Klassic Knee System - Revision Tibial Baseplate received FDA 510(k) clearance on 2025-03-24, under 510(k) number K243991.

Who is the listed applicant for Klassic Knee System - Revision Tibial Baseplate?

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

What is the FDA product code for Klassic Knee System - Revision Tibial Baseplate?

The FDA product code for Klassic Knee System - Revision Tibial Baseplate is JWH.

其他以 Total Joint Othopedics, 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：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。

K262057GMK 扩充設備Medacta International SA K260063GSPE 分隔器The General Hospital Corporation, d/b/a Massachusetts K262293EVOLUTION MPX™ 全膝系統Suzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ 全膝系統修復水泥固定胫骨增強器、樹枝擴展和壓入式樹枝擴展B-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK膝關節系統Just Medical Devices (Tianjin) Co., Ltd.

官方來源

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