植入式牙齒植體系統,植入式牙齒基座系統
K 號:K160221 · 2016-09-12
廣告
器材摘要
常見問題
What is the Implance Dental Implant System, Implance Dental Abutment System?
Implance Dental Implant System, Implance Dental Abutment System is a medical device that received FDA 510(k) clearance on 2016-09-12. The listed applicant is Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti.. The 510(k) number is K160221.
When did Implance Dental Implant System, Implance Dental Abutment System receive FDA 510(k) clearance?
Implance Dental Implant System, Implance Dental Abutment System received FDA 510(k) clearance on 2016-09-12, under 510(k) number K160221.
Who is the listed applicant for Implance Dental Implant System, Implance Dental Abutment System?
The FDA 510(k) record lists Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implance Dental Implant System, Implance Dental Abutment System?
The FDA product code for Implance Dental Implant System, Implance Dental Abutment System is DZE.
相關臨床試驗
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。
廣告