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FDA 510(k)

Vericore梯度临时盘

K号: K152443 · 2016-05-11

决定日期2016-05-11
产品代码EBG
咨询委员会DE 请注意,您没有提供具体的医疗设备监管文本内容,因此我无法进行翻译。请提供需要翻译的具体文本,我将根据您的要求进行翻译。
决定实质等同

器械摘要

Vericore Gradient Temporary Disc is the device name listed in this FDA 510(k) record. The listed applicant is Whip Mix Corporation. It received FDA 510(k) clearance on 2016-05-11 under 510(k) number K152443. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Vericore Gradient Temporary Disc?

Vericore Gradient Temporary Disc is a medical device that received FDA 510(k) clearance on 2016-05-11. The listed applicant is Whip Mix Corporation. The 510(k) number is K152443.

When did Vericore Gradient Temporary Disc receive FDA 510(k) clearance?

Vericore Gradient Temporary Disc received FDA 510(k) clearance on 2016-05-11, under 510(k) number K152443.

Who is the listed applicant for Vericore Gradient Temporary Disc?

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

What is the FDA product code for Vericore Gradient Temporary Disc?

The FDA product code for Vericore Gradient Temporary Disc is EBG.

相关临床试验

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。

列明Whip Mix Corporation为申报人的其他记录

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。

相关器械(代码:EBG)

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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