K-number	K213498
Device name	PELNAC Meshed Bilayer Wound Matrix
Applicant	Gunze Limited
Product code	KGN
Device class	Class U
Decision date	Jul 14, 2022
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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PELNAC Meshed Bilayer Wound Matrix

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