Trinity EVO 骨盆殼
K 號：K242744 · 2025-06-05
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器材摘要
Trinity EVO Acetabular Shell is the device name listed in this FDA 510(k) record. The listed applicant is Corin U.S.A. Limited. It received FDA 510(k) clearance on 2025-06-05 under 510(k) number K242744. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Trinity EVO Acetabular Shell?
Trinity EVO Acetabular Shell is a medical device that received FDA 510(k) clearance on 2025-06-05. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K242744.
When did Trinity EVO Acetabular Shell receive FDA 510(k) clearance?
Trinity EVO Acetabular Shell received FDA 510(k) clearance on 2025-06-05, under 510(k) number K242744.
Who is the listed applicant for Trinity EVO Acetabular Shell?
The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trinity EVO Acetabular Shell?
The FDA product code for Trinity EVO Acetabular Shell is LPH.
相關臨床試驗
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其他以 Corin U.S.A. Limited 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：LPH）
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
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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