K-number	K031402
Device name	PERFECTA FEMORAL STEM
Applicant	Wrightmedicaltechnologyinc
Product code	LPH
Device class	Class II
Decision date	Nov 22, 2004
Decision	Substantially Equivalent
Regulation	888.3358

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Source

View the full FDA submission: accessdata.fda.gov

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PERFECTA FEMORAL STEM

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