K-number	K210128
Device name	INTEGRA Wound Matrix (Macro-Channels)
Applicant	Integra LifeSciences Corporation
Product code	KGN
Device class	Class U
Decision date	Oct 8, 2021
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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INTEGRA Wound Matrix (Macro-Channels)

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