K-number	K960617
Device name	ADVANCE TIBIAL COMPONENT
Applicant	Wrightmedicaltechnologyinc
Product code	HRY
Device class	Class II
Decision date	May 8, 1996
Decision	Substantially Equivalent for Some Indications
Regulation	888.3530

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Source

View the full FDA submission: accessdata.fda.gov

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ADVANCE TIBIAL COMPONENT

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