InFill® 間隙融合設備
K 號:K172349 · 2017-12-14
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器材摘要
常見問題
What is the InFill® Interbody Fusion Device?
InFill® Interbody Fusion Device is a medical device that received FDA 510(k) clearance on 2017-12-14. The listed applicant is Pinnacle Spine Group, LLC. The 510(k) number is K172349.
When did InFill® Interbody Fusion Device receive FDA 510(k) clearance?
InFill® Interbody Fusion Device received FDA 510(k) clearance on 2017-12-14, under 510(k) number K172349.
Who is the listed applicant for InFill® Interbody Fusion Device?
The FDA 510(k) record lists Pinnacle Spine Group, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InFill® Interbody Fusion Device?
The FDA product code for InFill® Interbody Fusion Device 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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