K-number	K083150
Device name	G-FORCE TENODESIS SCREW
Applicant	Wrightmedicaltechnologyinc
Product code	MBI
Device class	Class II
Decision date	Jan 15, 2009
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 TENODESIS SCREW

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