NervAlign 神經袖套
K 號:K202234 · 2022-02-10
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器材摘要
常見問題
What is the NervAlign Nerve Cuff?
NervAlign Nerve Cuff is a medical device that received FDA 510(k) clearance on 2022-02-10. The listed applicant is Renerve, Ltd.. The 510(k) number is K202234.
When did NervAlign Nerve Cuff receive FDA 510(k) clearance?
NervAlign Nerve Cuff received FDA 510(k) clearance on 2022-02-10, under 510(k) number K202234.
Who is the listed applicant for NervAlign Nerve Cuff?
The FDA 510(k) record lists Renerve, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NervAlign Nerve Cuff?
The FDA product code for NervAlign Nerve Cuff is JXI.
相關臨床試驗
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:JXI)
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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