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FDA 510(k)

BILAYER MATRIX WOUND DRESSING

K-Number: K021792 · 2002-08-14

ApplicantIntegra Lifesciences Corp.
Decision Date2002-08-14
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

BILAYER MATRIX WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Integra Lifesciences Corp.. It received FDA 510(k) clearance on 2002-08-14 under 510(k) number K021792. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILAYER MATRIX WOUND DRESSING?

BILAYER MATRIX WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2002-08-14. The listed applicant is Integra Lifesciences Corp.. The 510(k) number is K021792.

When did BILAYER MATRIX WOUND DRESSING receive FDA 510(k) clearance?

BILAYER MATRIX WOUND DRESSING received FDA 510(k) clearance on 2002-08-14, under 510(k) number K021792.

Who is the listed applicant for BILAYER MATRIX WOUND DRESSING?

The FDA 510(k) record lists Integra Lifesciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BILAYER MATRIX WOUND DRESSING?

The FDA product code for BILAYER MATRIX WOUND DRESSING is KGN.

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Related Devices (Code: KGN)

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.

K260652ColActive PlusCovalon Technologies, Ltd.K260711Accelagen Plus Surgical Matrix, 1cc (CG-01AP);Accelagen Plus Surgical Matrix, 3cc (CG-03AP);Accelagen Plus Surgical Matrix, 5cc (CG-05AP);Accelagen Plus Surgical Strip, 125x25x2mm (CG-125X25AP);Accelagen Plus Surgical Strip, 250x25x2mm (CG-250X25AP)Berkeley Advanced BiomaterialsK260596Collagen Wound PowderVentris MedicalK260669Endoform Dermal TemplateAroa Biosurgery , Ltd.K253521ECMT-100 WMDEcm Therapeutics, Inc.K253204CatalyzeBioTissue Holdings, Inc.

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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