FDA 510(k)

Klockner牙槽

K号: K230103 · 2023-04-24

决定日期2023-04-24

产品代码NHA

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决定实质等同

器械摘要

Klockner Abutments 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 2023-04-24 under 510(k) number K230103. 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 Abutments?

Klockner Abutments is a medical device that received FDA 510(k) clearance on 2023-04-24. The listed applicant is SOADCO, S.L.. The 510(k) number is K230103.

When did Klockner Abutments receive FDA 510(k) clearance?

Klockner Abutments received FDA 510(k) clearance on 2023-04-24, under 510(k) number K230103.

Who is the listed applicant for Klockner Abutments?

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 Abutments?

The FDA product code for Klockner Abutments 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 K173642KLOCKNER 外科箱 K170022Klockner Vega TiBase for CEREC 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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官方来源

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