免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

MOR 3.0mm 及 PUR NP 3.2mm 嵌入系統,MOR 2.1x18mm 及 2.4x18mm

K 號:K171728 · 2017-09-28

決定日期2017-09-28
產品代碼DZE
諮詢委員會DE
決定相當於

器材摘要

MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm is the device name listed in this FDA 510(k) record. The listed applicant is Sterngold Dental, LLC. It received FDA 510(k) clearance on 2017-09-28 under 510(k) number K171728. 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 MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm?

MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm is a medical device that received FDA 510(k) clearance on 2017-09-28. The listed applicant is Sterngold Dental, LLC. The 510(k) number is K171728.

When did MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm receive FDA 510(k) clearance?

MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm received FDA 510(k) clearance on 2017-09-28, under 510(k) number K171728.

Who is the listed applicant for MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm?

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

What is the FDA product code for MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm?

The FDA product code for MOR 3.0mm and PUR NP 3.2mm Implant Systems, MOR 2.1x18mm and 2.4x18mm 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。

其他以 Sterngold Dental, LLC 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。

↑