Triathlon® 總膝系統 - Triathlon® Pro 後方穩定 (PS) 髋關節-component
K 號:K230952 · 2023-06-02
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器材摘要
常見問題
What is the Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component?
Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component is a medical device that received FDA 510(k) clearance on 2023-06-02. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K230952.
When did Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component receive FDA 510(k) clearance?
Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component received FDA 510(k) clearance on 2023-06-02, under 510(k) number K230952.
Who is the listed applicant for Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component?
The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component?
The FDA product code for Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component is JWH.
相關臨床試驗
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其他以 Howmedica Osteonics Corp., Dba Stryker Orthopaedics 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。
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。
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