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FDA 510(k)

VENTRIO HERNIA PATCH

K-Number: K100229 · 2010-04-21

ApplicantC.R. Bard, Inc.
Decision Date2010-04-21
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VENTRIO 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 2010-04-21 under 510(k) number K100229. 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 HERNIA PATCH?

VENTRIO HERNIA PATCH is a medical device that received FDA 510(k) clearance on 2010-04-21. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K100229.

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

VENTRIO HERNIA PATCH received FDA 510(k) clearance on 2010-04-21, under 510(k) number K100229.

Who is the listed applicant for VENTRIO 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 HERNIA PATCH?

The FDA product code for VENTRIO HERNIA PATCH is FTL.

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Related Devices (Code: 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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