XN膝關節人工關節系統
K 號：K232175 · 2024-04-14
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器材摘要
XN Knee Prosthesis System is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Chunlizhengda Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2024-04-14 under 510(k) number K232175. 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 XN Knee Prosthesis System?
XN Knee Prosthesis System is a medical device that received FDA 510(k) clearance on 2024-04-14. The listed applicant is Beijing Chunlizhengda Medical Instruments Co., Ltd.. The 510(k) number is K232175.
When did XN Knee Prosthesis System receive FDA 510(k) clearance?
XN Knee Prosthesis System received FDA 510(k) clearance on 2024-04-14, under 510(k) number K232175.
Who is the listed applicant for XN Knee Prosthesis System?
The FDA 510(k) record lists Beijing Chunlizhengda Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XN Knee Prosthesis System?
The FDA product code for XN Knee Prosthesis System is JWH.
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。
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。
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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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