K-number	K151437
Device name	ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug
Applicant	Atrium Medical Corporation
Product code	FTL
Device class	Class II
Decision date	Aug 27, 2015
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug

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