FDA 510(k)

CD HORIZON™ 穿孔螺釘組

K 號：K170347 · 2017-04-04

決定日期2017-04-04

產品代碼NKB

諮詢委員會或

決定相當於

器材摘要

CD HORIZON™ Fenestrated Screw Set is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek USA. It received FDA 510(k) clearance on 2017-04-04 under 510(k) number K170347. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CD HORIZON™ Fenestrated Screw Set?

CD HORIZON™ Fenestrated Screw Set is a medical device that received FDA 510(k) clearance on 2017-04-04. The listed applicant is Medtronic Sofamor Danek USA. The 510(k) number is K170347.

When did CD HORIZON™ Fenestrated Screw Set receive FDA 510(k) clearance?

CD HORIZON™ Fenestrated Screw Set received FDA 510(k) clearance on 2017-04-04, under 510(k) number K170347.

Who is the listed applicant for CD HORIZON™ Fenestrated Screw Set?

The FDA 510(k) record lists Medtronic Sofamor Danek USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CD HORIZON™ Fenestrated Screw Set?

The FDA product code for CD HORIZON™ Fenestrated Screw Set is NKB.

其他以 Medtronic Sofamor Danek USA 為申請人之記錄

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相關器械（代碼：NKB）

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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