膝+
K 號：K220104 · 2022-09-01
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器材摘要
Knee+ is the device name listed in this FDA 510(k) record. The listed applicant is Pixee Medical. It received FDA 510(k) clearance on 2022-09-01 under 510(k) number K220104. The device is classified under product code SBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Knee+?
Knee+ is a medical device that received FDA 510(k) clearance on 2022-09-01. The listed applicant is Pixee Medical. The 510(k) number is K220104.
When did Knee+ receive FDA 510(k) clearance?
Knee+ received FDA 510(k) clearance on 2022-09-01, under 510(k) number K220104.
Who is the listed applicant for Knee+?
The FDA 510(k) record lists Pixee Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Knee+?
The FDA product code for Knee+ is SBF.
其他以 Pixee Medical 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：SBF）
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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