FDA 510(k)

NUVO IF 种植系统

K号: K193234 · 2020-06-18

申请人Jjgc Industria E Comercio DE Materiais Dentarios S.A.

决定日期2020-06-18

产品代码DZE

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决定实质等同

器械摘要

NUVO IF Implant System 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 2020-06-18 under 510(k) number K193234. 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 NUVO IF Implant System?

NUVO IF Implant System is a medical device that received FDA 510(k) clearance on 2020-06-18. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K193234.

When did NUVO IF Implant System receive FDA 510(k) clearance?

NUVO IF Implant System received FDA 510(k) clearance on 2020-06-18, under 510(k) number K193234.

Who is the listed applicant for NUVO IF Implant System?

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 NUVO IF Implant System?

The FDA product code for NUVO IF Implant System is DZE.

列明Jjgc Industria E Comercio DE Materiais Dentarios S.A.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。

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