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FDA 510(k)

NuVasive Lumbar Interbody Implants

K号: K161230 · 2016-08-25

决定日期2016-08-25
产品代码MAX
咨询委员会OR
决定Substantially Equivalent

器械摘要

NuVasive Lumbar Interbody Implants 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 2016-08-25 under 510(k) number K161230. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NuVasive Lumbar Interbody Implants?

NuVasive Lumbar Interbody Implants is a medical device that received FDA 510(k) clearance on 2016-08-25. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K161230.

When did NuVasive Lumbar Interbody Implants receive FDA 510(k) clearance?

NuVasive Lumbar Interbody Implants received FDA 510(k) clearance on 2016-08-25, under 510(k) number K161230.

Who is the listed applicant for NuVasive Lumbar Interbody Implants?

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 Lumbar Interbody Implants?

The FDA product code for NuVasive Lumbar Interbody Implants is MAX.

相关临床试验

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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:MAX)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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