K-number	K213607
Device name	Geistlich Wound Matrix PLUS
Applicant	Geistlich Pharma AG
Product code	KGN
Device class	Class U
Decision date	Apr 28, 2022
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Geistlich Wound Matrix PLUS

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