合規樹枝擴展線，#0
K 號：K243466 · 2025-01-06
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器材摘要
Conformity Stem Extension Line, #0 is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2025-01-06 under 510(k) number K243466. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Conformity Stem Extension Line, #0?
Conformity Stem Extension Line, #0 is a medical device that received FDA 510(k) clearance on 2025-01-06. The listed applicant is United Orthopedic Corporation. The 510(k) number is K243466.
When did Conformity Stem Extension Line, #0 receive FDA 510(k) clearance?
Conformity Stem Extension Line, #0 received FDA 510(k) clearance on 2025-01-06, under 510(k) number K243466.
Who is the listed applicant for Conformity Stem Extension Line, #0?
FDA 510(k) 記錄中將 United Orthopedic Corporation 列為申請人。這並不單獨確立該設備製造商的身份。
What is the FDA product code for Conformity Stem Extension Line, #0?
The FDA product code for Conformity Stem Extension Line, #0 is LZO.
相關臨床試驗
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。
其他以 United Orthopedic Corporation 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：LZO）
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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