SD 牙槽橋
K 號：K173570 · 2019-05-17
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器材摘要
SD Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Surgident Co., Ltd.. It received FDA 510(k) clearance on 2019-05-17 under 510(k) number K173570. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SD Abutment?
SD Abutment is a medical device that received FDA 510(k) clearance on 2019-05-17. The listed applicant is Surgident Co., Ltd.. The 510(k) number is K173570.
When did SD Abutment receive FDA 510(k) clearance?
SD Abutment received FDA 510(k) clearance on 2019-05-17, under 510(k) number K173570.
Who is the listed applicant for SD Abutment?
The FDA 510(k) record lists Surgident Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SD Abutment?
The FDA product code for SD Abutment is NHA.
相關臨床試驗
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相關器械（代碼：NHA）
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
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