K-number	K100579
Device name	G-FORCE TI SUTURE ANCHOR SYSTEM
Applicant	Wrightmedicaltechnologyinc
Product code	MBI
Device class	Class II
Decision date	Mar 26, 2010
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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G-FORCE TI SUTURE ANCHOR SYSTEM

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