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FDA 510(k)

COATED VICRYL* (POLYGLACTIN 910) SUTURE

K-Number: K022269 · 2002-09-13

ApplicantETHICON, Inc.
Decision Date2002-09-13
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COATED VICRYL* (POLYGLACTIN 910) SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2002-09-13 under 510(k) number K022269. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COATED VICRYL* (POLYGLACTIN 910) SUTURE?

COATED VICRYL* (POLYGLACTIN 910) SUTURE is a medical device that received FDA 510(k) clearance on 2002-09-13. The listed applicant is ETHICON, Inc.. The 510(k) number is K022269.

When did COATED VICRYL* (POLYGLACTIN 910) SUTURE receive FDA 510(k) clearance?

COATED VICRYL* (POLYGLACTIN 910) SUTURE received FDA 510(k) clearance on 2002-09-13, under 510(k) number K022269.

Who is the listed applicant for COATED VICRYL* (POLYGLACTIN 910) SUTURE?

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 COATED VICRYL* (POLYGLACTIN 910) SUTURE?

The FDA product code for COATED VICRYL* (POLYGLACTIN 910) SUTURE is GAM.

Related Clinical Trials

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.

Other records listing ETHICON, Inc. as applicant

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.

View all 195 devices →

Related Devices (Code: GAM)

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.

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.

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