K-number	K121890
Device name	GENESYS PRESSFT SUTURE ANCHOR
Applicant	Linvatec Corporation D/B/A Conmed Linvatec
Product code	MAI
Device class	Class II
Decision date	Aug 22, 2012
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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GENESYS PRESSFT SUTURE ANCHOR

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