自訂骨固定/骨增強系統 - PIN
K 號:K243190 · 2025-06-27
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器材摘要
常見問題
What is the USTOMED Bone Fixation/Bone Augmentation Systems - PIN?
USTOMED Bone Fixation/Bone Augmentation Systems - PIN is a medical device that received FDA 510(k) clearance on 2025-06-27. The listed applicant is Ustomed Instrumente Ulrich Storz GmbH & Co. KG. The 510(k) number is K243190.
When did USTOMED Bone Fixation/Bone Augmentation Systems - PIN receive FDA 510(k) clearance?
USTOMED Bone Fixation/Bone Augmentation Systems - PIN received FDA 510(k) clearance on 2025-06-27, under 510(k) number K243190.
Who is the listed applicant for USTOMED Bone Fixation/Bone Augmentation Systems - PIN?
The FDA 510(k) record lists Ustomed Instrumente Ulrich Storz GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for USTOMED Bone Fixation/Bone Augmentation Systems - PIN?
The FDA product code for USTOMED Bone Fixation/Bone Augmentation Systems - PIN is DZL.
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相關器械(代碼:DZL)
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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