K-number	K003984
Device name	SUPER REVO SUTURE ANCHOR
Applicant	Linvatec Corp.
Product code	MAI
Device class	Class II
Decision date	Mar 19, 2001
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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SUPER REVO SUTURE ANCHOR

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