Bendini雲應用程序
K 號：K233706 · 2024-08-02
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器材摘要
Bendini Cloud Application is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive. It received FDA 510(k) clearance on 2024-08-02 under 510(k) number K233706. 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 Bendini Cloud Application?
Bendini Cloud Application is a medical device that received FDA 510(k) clearance on 2024-08-02. The listed applicant is Nuvasive. The 510(k) number is K233706.
When did Bendini Cloud Application receive FDA 510(k) clearance?
Bendini Cloud Application received FDA 510(k) clearance on 2024-08-02, under 510(k) number K233706.
Who is the listed applicant for Bendini Cloud Application?
The FDA 510(k) record lists Nuvasive as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bendini Cloud Application?
The FDA product code for Bendini Cloud Application is OLO.
相關臨床試驗
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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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