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FDA 510(k)

NuVasive CoRoent Small Ti-C System

K号: K162138 · 2016-10-26

决定日期2016-10-26
产品代码ODP
咨询委员会OR
决定Substantially Equivalent

器械摘要

NuVasive CoRoent Small Ti-C System is the device name listed in this FDA 510(k) record. The listed applicant is Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2016-10-26 under 510(k) number K162138. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NuVasive CoRoent Small Ti-C System?

NuVasive CoRoent Small Ti-C System is a medical device that received FDA 510(k) clearance on 2016-10-26. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K162138.

When did NuVasive CoRoent Small Ti-C System receive FDA 510(k) clearance?

NuVasive CoRoent Small Ti-C System received FDA 510(k) clearance on 2016-10-26, under 510(k) number K162138.

Who is the listed applicant for NuVasive CoRoent Small Ti-C System?

The FDA 510(k) record lists Nu Vasive, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NuVasive CoRoent Small Ti-C System?

The FDA product code for NuVasive CoRoent Small Ti-C System is ODP.

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列明Nu Vasive, Incorporated为申报人的其他记录

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相关器械(代码:ODP)

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