JuggerKnot 轟結式軟性固定器
K 號：K231128 · 2023-05-17
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器材摘要
JuggerKnot Soft Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2023-05-17 under 510(k) number K231128. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the JuggerKnot Soft Anchor?
JuggerKnot Soft Anchor is a medical device that received FDA 510(k) clearance on 2023-05-17. The listed applicant is Riverpoint Medical, LLC. The 510(k) number is K231128.
When did JuggerKnot Soft Anchor receive FDA 510(k) clearance?
JuggerKnot Soft Anchor received FDA 510(k) clearance on 2023-05-17, under 510(k) number K231128.
Who is the listed applicant for JuggerKnot Soft Anchor?
The FDA 510(k) record lists Riverpoint Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JuggerKnot Soft Anchor?
The FDA product code for JuggerKnot Soft Anchor is MBI.
相關臨床試驗
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其他以 Riverpoint Medical, LLC 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：MBI）
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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