DynaMesh-VENTRAL
K-Number: K161550 · 2016-12-22
Decision Date2016-12-22
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
DynaMesh-VENTRAL is a medical device manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. It received FDA 510(k) clearance on 2016-12-22 under approval number K161550. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DynaMesh-VENTRAL?
DynaMesh-VENTRAL is a medical device that received FDA 510(k) clearance on 2016-12-22. It is manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. The 510(k) number is K161550.
When was DynaMesh-VENTRAL approved by the FDA?
DynaMesh-VENTRAL received FDA 510(k) clearance on 2016-12-22, under approval number K161550.
What company makes DynaMesh-VENTRAL?
DynaMesh-VENTRAL is manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft.
What is the FDA product code for DynaMesh-VENTRAL?
The FDA product code for DynaMesh-VENTRAL is FTL.
Other Devices by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.