FDA 510(k)

디나메시-벤트럴

K-번호: K161550 · 2016-12-22

신청자Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft

결정일2016-12-22

제품 코드FTL

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

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기기 요약

DynaMesh-VENTRAL 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 2016-12-22 under 510(k) number K161550. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the DynaMesh-VENTRAL?

DynaMesh-VENTRAL is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. The 510(k) number is K161550.

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

DynaMesh-VENTRAL received FDA 510(k) clearance on 2016-12-22, under 510(k) number K161550.

Who is the listed applicant for DynaMesh-VENTRAL?

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-VENTRAL?

The FDA product code for DynaMesh-VENTRAL is FTL.

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