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FDA 510(k)

颧骨植入物

K号: K190718 · 2019-07-11

决定日期2019-07-11
产品代码DZE
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

Zygomatic Implants is the device name listed in this FDA 510(k) record. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2019-07-11 under 510(k) number K190718. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Zygomatic Implants?

Zygomatic Implants is a medical device that received FDA 510(k) clearance on 2019-07-11. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K190718.

When did Zygomatic Implants receive FDA 510(k) clearance?

Zygomatic Implants received FDA 510(k) clearance on 2019-07-11, under 510(k) number K190718.

Who is the listed applicant for Zygomatic Implants?

The FDA 510(k) record lists Jjgc Industria E Comercio DE Materiais Dentarios S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zygomatic Implants?

The FDA product code for Zygomatic Implants is DZE.

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列明Jjgc Industria E Comercio DE Materiais Dentarios S.A.为申报人的其他记录

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相关器械(代码:DZE)

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。

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