FDA 510(k)

征服FN

K 號：K172785 · 2017-12-22

決定日期2017-12-22

產品代碼JDO

諮詢委員會或

決定相當於

器材摘要

CONQUEST FN is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew. It received FDA 510(k) clearance on 2017-12-22 under 510(k) number K172785. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CONQUEST FN?

CONQUEST FN is a medical device that received FDA 510(k) clearance on 2017-12-22. The listed applicant is Smith & Nephew. The 510(k) number is K172785.

When did CONQUEST FN receive FDA 510(k) clearance?

CONQUEST FN received FDA 510(k) clearance on 2017-12-22, under 510(k) number K172785.

Who is the listed applicant for CONQUEST FN?

The FDA 510(k) record lists Smith & Nephew as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONQUEST FN?

The FDA product code for CONQUEST FN is JDO.

其他以 Smith & Nephew 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。

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相關器械（代碼：JDO）

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。

K230764骨心整合髋關節固定系統OsteoCentric Technologies K213126史密斯與內夫公司，板和螺釘系統：EVOS、Peri-Loc、D-Rad、TC-100、VLP Mini-Mod、壓縮髋螺釘（CHS）、CONQUEST FN 及針筒螺釘Smith & Nephew, Inc.K210247骨心整合髋關節固定系統Osteocentric Technologies D.B.A. Osteocentric Trauma K193029征服FNSmith & Nephew, Inc.K173826THP 髋部骨折板系統Biomet, Inc.K152686征服FNSmith & Nephew

官方來源

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