FDA 510(k)

Ritter 牙科植入系统

K号: K160475 · 2016-12-14

决定日期2016-12-14

产品代码DZE

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决定实质等同

器械摘要

Ritter Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Ritter Implants GmbH & Co. KG. It received FDA 510(k) clearance on 2016-12-14 under 510(k) number K160475. 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 Ritter Dental Implant System?

Ritter Dental Implant System is a medical device that received FDA 510(k) clearance on 2016-12-14. The listed applicant is Ritter Implants GmbH & Co. KG. The 510(k) number is K160475.

When did Ritter Dental Implant System receive FDA 510(k) clearance?

Ritter Dental Implant System received FDA 510(k) clearance on 2016-12-14, under 510(k) number K160475.

Who is the listed applicant for Ritter Dental Implant System?

The FDA 510(k) record lists Ritter Implants GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ritter Dental Implant System?

The FDA product code for Ritter Dental Implant System is DZE.

列明Ritter Implants GmbH & Co. KG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。

K180183Ritter 牙科植入系统

官方来源

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