FDA 510(k)

Klockner Vega TiBase for CEREC

K号: K170022 · 2017-11-16

决定日期2017-11-16

产品代码NHA

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决定实质等同

器械摘要

Klockner Vega TiBase for CEREC is the device name listed in this FDA 510(k) record. The listed applicant is SOADCO, S.L.. It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K170022. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Klockner Vega TiBase for CEREC?

Klockner Vega TiBase for CEREC is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is SOADCO, S.L.. The 510(k) number is K170022.

When did Klockner Vega TiBase for CEREC receive FDA 510(k) clearance?

Klockner Vega TiBase for CEREC received FDA 510(k) clearance on 2017-11-16, under 510(k) number K170022.

Who is the listed applicant for Klockner Vega TiBase for CEREC?

The FDA 510(k) record lists SOADCO, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Klockner Vega TiBase for CEREC?

The FDA product code for Klockner Vega TiBase for CEREC is NHA.

列明SOADCO, S.L.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。

K243128Klockner套件 K230103Klockner牙槽 K173642KLOCKNER 外科箱 K153098KLOCKNER VEGA 牙科植入系统 K151194KLOCKNER 牙科植入体基座（II）

相关器械（代码：NHA）

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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