FDA 510(k)

IPS e.max® Press牙冠解决方案适用于Viteo Base Ti

K号: K160798 · 2016-12-15

决定日期2016-12-15

产品代码NHA

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决定实质等同

器械摘要

IPS e.max® Press Abutment Solutions for Viteo Base Ti is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, AG. It received FDA 510(k) clearance on 2016-12-15 under 510(k) number K160798. 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 IPS e.max® Press Abutment Solutions for Viteo Base Ti?

IPS e.max® Press Abutment Solutions for Viteo Base Ti is a medical device that received FDA 510(k) clearance on 2016-12-15. The listed applicant is Ivoclar Vivadent, AG. The 510(k) number is K160798.

When did IPS e.max® Press Abutment Solutions for Viteo Base Ti receive FDA 510(k) clearance?

IPS e.max® Press Abutment Solutions for Viteo Base Ti received FDA 510(k) clearance on 2016-12-15, under 510(k) number K160798.

Who is the listed applicant for IPS e.max® Press Abutment Solutions for Viteo Base Ti?

The FDA 510(k) record lists Ivoclar Vivadent, AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPS e.max® Press Abutment Solutions for Viteo Base Ti?

The FDA product code for IPS e.max® Press Abutment Solutions for Viteo Base Ti is NHA.

列明Ivoclar Vivadent, AG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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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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