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)

N1 TiUltra TCC 偽裝系統

K 號:K211109 · 2021-12-21

決定日期2021-12-21
產品代碼DZE
諮詢委員會DE
決定相當於

器材摘要

N1 TiUltra TCC Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare Services AG. It received FDA 510(k) clearance on 2021-12-21 under 510(k) number K211109. 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 N1 TiUltra TCC Implant System?

N1 TiUltra TCC Implant System is a medical device that received FDA 510(k) clearance on 2021-12-21. The listed applicant is Nobel Biocare Services AG. The 510(k) number is K211109.

When did N1 TiUltra TCC Implant System receive FDA 510(k) clearance?

N1 TiUltra TCC Implant System received FDA 510(k) clearance on 2021-12-21, under 510(k) number K211109.

Who is the listed applicant for N1 TiUltra TCC Implant System?

The FDA 510(k) record lists Nobel Biocare Services AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N1 TiUltra TCC Implant System?

The FDA product code for N1 TiUltra TCC Implant 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。

其他以 Nobel Biocare Services 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。

↑