科傾側方椎間體系
K 號:K151406 · 2016-02-25
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器材摘要
常見問題
What is the Cogent Lateral Interbody System?
Cogent Lateral Interbody System is a medical device that received FDA 510(k) clearance on 2016-02-25. The listed applicant is Cogent Spine, LLC. The 510(k) number is K151406.
When did Cogent Lateral Interbody System receive FDA 510(k) clearance?
Cogent Lateral Interbody System received FDA 510(k) clearance on 2016-02-25, under 510(k) number K151406.
Who is the listed applicant for Cogent Lateral Interbody System?
The FDA 510(k) record lists Cogent Spine, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cogent Lateral Interbody System?
The FDA product code for Cogent Lateral Interbody System is MAX.
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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。
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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