DynaMesh-POSTERIOR
K-Number: K182087 · 2018-10-31
Decision Date2018-10-31
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
DynaMesh-POSTERIOR is a medical device manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. It received FDA 510(k) clearance on 2018-10-31 under approval number K182087. 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-POSTERIOR?
DynaMesh-POSTERIOR is a medical device that received FDA 510(k) clearance on 2018-10-31. It is manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft. The 510(k) number is K182087.
When was DynaMesh-POSTERIOR approved by the FDA?
DynaMesh-POSTERIOR received FDA 510(k) clearance on 2018-10-31, under approval number K182087.
What company makes DynaMesh-POSTERIOR?
DynaMesh-POSTERIOR is manufactured by Feg Textiltechnik Forschungs- Und Entwicklungsgesellschaft.
What is the FDA product code for DynaMesh-POSTERIOR?
The FDA product code for DynaMesh-POSTERIOR 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.