K-number	K111233
Device name	SUPRIS RETROPUBIC SLING SYSTEM
Applicant	Coloplast A/S
Product code	OTN
Device class	Class II
Decision date	Jun 24, 2011
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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SUPRIS RETROPUBIC SLING SYSTEM

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