紅色® AL-T
K 號：K242589 · 2024-10-23
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器材摘要
Scarlet® AL-T is the device name listed in this FDA 510(k) record. The listed applicant is Spineart SA. It received FDA 510(k) clearance on 2024-10-23 under 510(k) number K242589. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Scarlet® AL-T?
Scarlet® AL-T is a medical device that received FDA 510(k) clearance on 2024-10-23. The listed applicant is Spineart SA. The 510(k) number is K242589.
When did Scarlet® AL-T receive FDA 510(k) clearance?
Scarlet® AL-T received FDA 510(k) clearance on 2024-10-23, under 510(k) number K242589.
Who is the listed applicant for Scarlet® AL-T?
FDA 510(k) 記錄將 Spineart SA 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Scarlet® AL-T?
The FDA product code for Scarlet® AL-T is MAX.
相關臨床試驗
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其他以 Spineart SA 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：MAX）
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。
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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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