膝聲軟骨評估系統（750-3600-001）
K 號：K252076 · 2026-02-06
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器材摘要
Kneevoice Cartilage Evaluation System (750-3600-001) is the device name listed in this FDA 510(k) record. The listed applicant is Kneevoice, Inc.. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K252076. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Kneevoice Cartilage Evaluation System (750-3600-001)?
Kneevoice Cartilage Evaluation System (750-3600-001) is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Kneevoice, Inc.. The 510(k) number is K252076.
When did Kneevoice Cartilage Evaluation System (750-3600-001) receive FDA 510(k) clearance?
Kneevoice Cartilage Evaluation System (750-3600-001) received FDA 510(k) clearance on 2026-02-06, under 510(k) number K252076.
Who is the listed applicant for Kneevoice Cartilage Evaluation System (750-3600-001)?
The FDA 510(k) record lists Kneevoice, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001)?
The FDA product code for Kneevoice Cartilage Evaluation System (750-3600-001) is DQD.
相關臨床試驗
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相關器械（代碼：DQD）
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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