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FDA 510(k)

薩維恩營地螺釘系統

K 號:K161857 · 2017-04-28

決定日期2017-04-28
產品代碼DZL
諮詢委員會DE
決定相當於

器材摘要

Salvin Tenting Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Salvin Dental Specialties. It received FDA 510(k) clearance on 2017-04-28 under 510(k) number K161857. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Salvin Tenting Screw System?

Salvin Tenting Screw System is a medical device that received FDA 510(k) clearance on 2017-04-28. The listed applicant is Salvin Dental Specialties. The 510(k) number is K161857.

When did Salvin Tenting Screw System receive FDA 510(k) clearance?

Salvin Tenting Screw System received FDA 510(k) clearance on 2017-04-28, under 510(k) number K161857.

Who is the listed applicant for Salvin Tenting Screw System?

The FDA 510(k) record lists Salvin Dental Specialties as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Salvin Tenting Screw System?

The FDA product code for Salvin Tenting Screw System is DZL.

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。

其他以 Salvin Dental Specialties 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: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

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