FDA 510(k)

In2Bones 賈辛格針

K 號：K153204 · 2016-02-01

決定日期2016-02-01

產品代碼HTY

諮詢委員會或

決定相當於

器材摘要

In2Bones Kirschner wire is the device name listed in this FDA 510(k) record. The listed applicant is In2bones Sas. It received FDA 510(k) clearance on 2016-02-01 under 510(k) number K153204. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the In2Bones Kirschner wire?

In2Bones Kirschner wire is a medical device that received FDA 510(k) clearance on 2016-02-01. The listed applicant is In2bones Sas. The 510(k) number is K153204.

When did In2Bones Kirschner wire receive FDA 510(k) clearance?

In2Bones Kirschner wire received FDA 510(k) clearance on 2016-02-01, under 510(k) number K153204.

Who is the listed applicant for In2Bones Kirschner wire?

The FDA 510(k) record lists In2bones Sas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for In2Bones Kirschner wire?

The FDA product code for In2Bones Kirschner wire is HTY.

其他以 In2bones Sas 為申請人之記錄

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相關器械（代碼：HTY）

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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