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FDA 510(k)

VICRYL Mesh

K-Number: K201143 · 2020-08-06

ApplicantETHICON, Inc.
Decision Date2020-08-06
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VICRYL Mesh is a medical device manufactured by ETHICON, Inc.. It received FDA 510(k) clearance on 2020-08-06 under approval number K201143. 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 VICRYL Mesh?

VICRYL Mesh is a medical device that received FDA 510(k) clearance on 2020-08-06. It is manufactured by ETHICON, Inc.. The 510(k) number is K201143.

When was VICRYL Mesh approved by the FDA?

VICRYL Mesh received FDA 510(k) clearance on 2020-08-06, under approval number K201143.

What company makes VICRYL Mesh?

VICRYL Mesh is manufactured by ETHICON, Inc..

What is the FDA product code for VICRYL Mesh?

The FDA product code for VICRYL Mesh is FTL.

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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.

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