斯特羅曼骨水平針狹型植體
K 號：K153758 · 2016-03-23
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器材摘要
Straumann Bone Level Tapered Implants is the device name listed in this FDA 510(k) record. The listed applicant is Institut Straumann AG. It received FDA 510(k) clearance on 2016-03-23 under 510(k) number K153758. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Straumann Bone Level Tapered Implants?
Straumann Bone Level Tapered Implants is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Institut Straumann AG. The 510(k) number is K153758.
When did Straumann Bone Level Tapered Implants receive FDA 510(k) clearance?
Straumann Bone Level Tapered Implants received FDA 510(k) clearance on 2016-03-23, under 510(k) number K153758.
Who is the listed applicant for Straumann Bone Level Tapered Implants?
The FDA 510(k) record lists Institut Straumann AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Straumann Bone Level Tapered Implants?
The FDA product code for Straumann Bone Level Tapered Implants is DZE.
相關臨床試驗
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其他以 Institut Straumann AG 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：DZE）
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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