K-number	K221556
Device name	T-Line Hernia Mesh
Applicant	Deep Blue Medical Advances, Inc.
Product code	FTL
Device class	Class II
Decision date	Nov 28, 2022
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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T-Line Hernia Mesh

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