K-number	K033529
Device name	TIE-IN TRAPEZIUM
Applicant	Wrightmedicaltechnologyinc
Product code	KYI
Device class	Class II
Decision date	Dec 3, 2003
Decision	Substantially Equivalent
Regulation	888.3770

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View the full FDA submission: accessdata.fda.gov

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TIE-IN TRAPEZIUM

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