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FDA 510(k)

BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH

K-Number: K031332 · 2003-05-15

ApplicantC.R. Bard, Inc.
Decision Date2003-05-15
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH 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 2003-05-15 under 510(k) number K031332. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH?

BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH is a medical device that received FDA 510(k) clearance on 2003-05-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K031332.

When did BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH receive FDA 510(k) clearance?

BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH received FDA 510(k) clearance on 2003-05-15, under 510(k) number K031332.

Who is the listed applicant for BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH?

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 BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH?

The FDA product code for BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH is FTM.

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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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