FDA 510(k)

DynaMesh-POSTERIOR

K号: K182087 · 2018-10-31

申请人Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft

决定日期2018-10-31

产品代码FTL

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决定实质等同

器械摘要

DynaMesh-POSTERIOR is the device name listed in this FDA 510(k) record. The listed applicant is Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. It received FDA 510(k) clearance on 2018-10-31 under 510(k) number K182087. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DynaMesh-POSTERIOR?

DynaMesh-POSTERIOR is a medical device that received FDA 510(k) clearance on 2018-10-31. The listed applicant is Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. The 510(k) number is K182087.

When did DynaMesh-POSTERIOR receive FDA 510(k) clearance?

DynaMesh-POSTERIOR received FDA 510(k) clearance on 2018-10-31, under 510(k) number K182087.

Who is the listed applicant for DynaMesh-POSTERIOR?

The FDA 510(k) record lists Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DynaMesh-POSTERIOR?

The FDA product code for DynaMesh-POSTERIOR is FTL.

列明Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft为申报人的其他记录

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K161550DynaMesh-VENTRAL

官方来源

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