FDA 510(k)

GalaFORM 3D

K号: K162922 · 2017-02-23

决定日期2017-02-23

产品代码OOD

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决定实质等同

器械摘要

GalaFORM 3D is the device name listed in this FDA 510(k) record. The listed applicant is Tepha, Inc.. It received FDA 510(k) clearance on 2017-02-23 under 510(k) number K162922. The device is classified under product code OOD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the GalaFORM 3D?

GalaFORM 3D is a medical device that received FDA 510(k) clearance on 2017-02-23. The listed applicant is Tepha, Inc.. The 510(k) number is K162922.

When did GalaFORM 3D receive FDA 510(k) clearance?

GalaFORM 3D received FDA 510(k) clearance on 2017-02-23, under 510(k) number K162922.

Who is the listed applicant for GalaFORM 3D?

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

What is the FDA product code for GalaFORM 3D?

The FDA product code for GalaFORM 3D is OOD.

列明Tepha, 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。

K233999GalaFLEX LITE支架 K202425SurgiLattice scaffold K211307GalaSTITCH 吸收性单丝缝合线 K161092GalaSHAPE 3D

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