FDA 510(k)

RODO牙支持系统

K号: K160786 · 2016-11-21

决定日期2016-11-21

产品代码NHA

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决定实质等同

器械摘要

RODO Abutment System is the device name listed in this FDA 510(k) record. The listed applicant is Rodo Medical, Inc.. It received FDA 510(k) clearance on 2016-11-21 under 510(k) number K160786. 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 RODO Abutment System?

RODO Abutment System is a medical device that received FDA 510(k) clearance on 2016-11-21. The listed applicant is Rodo Medical, Inc.. The 510(k) number is K160786.

When did RODO Abutment System receive FDA 510(k) clearance?

RODO Abutment System received FDA 510(k) clearance on 2016-11-21, under 510(k) number K160786.

Who is the listed applicant for RODO Abutment System?

The FDA 510(k) record lists Rodo Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RODO Abutment System?

The FDA product code for RODO Abutment System is NHA.

列明Rodo Medical, Inc.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。

K193274Rodo 支撑系统 K180609Rodo Smilekey

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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