FDA 510(k)

VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING

K-Number: K113229 · 2012-07-20

Decision Date2012-07-20

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2012-07-20 under 510(k) number K113229. 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 VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING?

VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING is a medical device that received FDA 510(k) clearance on 2012-07-20. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K113229.

When did VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING receive FDA 510(k) clearance?

VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING received FDA 510(k) clearance on 2012-07-20, under 510(k) number K113229.

Who is the listed applicant for VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING?

The FDA product code for VENTRIO LIGHT HERNIA PATCH WITH TRM ANTIMICROBIAL COATING is FTL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.