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FDA 510(k)

VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH

K-Number: K851086 · 1985-05-21

ApplicantETHICON, Inc.
Decision Date1985-05-21
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K851086. 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 VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH?

VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is ETHICON, Inc.. The 510(k) number is K851086.

When did VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH receive FDA 510(k) clearance?

VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851086.

Who is the listed applicant for VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH?

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 (POLYGLACTIN 910/MERSILENE COMPOISITE MESH?

The FDA product code for VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH is FTM.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: 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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