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)

MIS CONNECT 圆錐連接基座

K 號:K173326 · 2018-03-16

決定日期2018-03-16
產品代碼NHA
諮詢委員會DE
決定相當於

器材摘要

MIS CONNECT Conical Connection Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Mis Implants Technologies , Ltd.. It received FDA 510(k) clearance on 2018-03-16 under 510(k) number K173326. 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 MIS CONNECT Conical Connection Abutment?

MIS CONNECT Conical Connection Abutment is a medical device that received FDA 510(k) clearance on 2018-03-16. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K173326.

When did MIS CONNECT Conical Connection Abutment receive FDA 510(k) clearance?

MIS CONNECT Conical Connection Abutment received FDA 510(k) clearance on 2018-03-16, under 510(k) number K173326.

Who is the listed applicant for MIS CONNECT Conical Connection Abutment?

The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIS CONNECT Conical Connection Abutment?

The FDA product code for MIS CONNECT Conical Connection Abutment is NHA.

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 Mis Implants Technologies , Ltd. 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: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。

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。

↑