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FDA 510(k)

VICRYL * MESH BAG

K-Number: K051701 · 2005-09-29

ApplicantETHICON, Inc.
Decision Date2005-09-29
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VICRYL * MESH BAG is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2005-09-29 under 510(k) number K051701. 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 BAG?

VICRYL * MESH BAG is a medical device that received FDA 510(k) clearance on 2005-09-29. The listed applicant is ETHICON, Inc.. The 510(k) number is K051701.

When did VICRYL * MESH BAG receive FDA 510(k) clearance?

VICRYL * MESH BAG received FDA 510(k) clearance on 2005-09-29, under 510(k) number K051701.

Who is the listed applicant for VICRYL * MESH BAG?

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

What is the FDA product code for VICRYL * MESH BAG?

The FDA product code for VICRYL * MESH BAG is FTL.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: FTL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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