iASSIST 適合膝關節系統
K 號：K213033 · 2022-01-14
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器材摘要
iASSIST Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Orthosoft D/B/A Zimmer Cas. It received FDA 510(k) clearance on 2022-01-14 under 510(k) number K213033. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the iASSIST Knee System?
iASSIST Knee System is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Orthosoft D/B/A Zimmer Cas. The 510(k) number is K213033.
When did iASSIST Knee System receive FDA 510(k) clearance?
iASSIST Knee System received FDA 510(k) clearance on 2022-01-14, under 510(k) number K213033.
Who is the listed applicant for iASSIST Knee System?
The FDA 510(k) record lists Orthosoft D/B/A Zimmer Cas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iASSIST Knee System?
The FDA product code for iASSIST Knee System is OLO.
相關臨床試驗
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其他以 Orthosoft D/B/A Zimmer Cas 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：OLO）
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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