FDA 510(k)

VENTRIO ST HERNIA PATCH

K-Number: K101920 · 2011-03-23

Decision Date2011-03-23

Product CodeFTL

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VENTRIO ST HERNIA PATCH 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 2011-03-23 under 510(k) number K101920. 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 ST HERNIA PATCH?

VENTRIO ST HERNIA PATCH is a medical device that received FDA 510(k) clearance on 2011-03-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K101920.

When did VENTRIO ST HERNIA PATCH receive FDA 510(k) clearance?

VENTRIO ST HERNIA PATCH received FDA 510(k) clearance on 2011-03-23, under 510(k) number K101920.

Who is the listed applicant for VENTRIO ST HERNIA PATCH?

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 ST HERNIA PATCH?

The FDA product code for VENTRIO ST HERNIA PATCH 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.