K-number	K080663
Device name	PROFEMUR LX REVISION 5/8 COATED HIP STEM
Applicant	Wrightmedicaltechnologyinc
Product code	KWA
Device class	Class III
Decision date	Apr 8, 2008
Decision	Substantially Equivalent
Regulation	888.3330

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Source

View the full FDA submission: accessdata.fda.gov

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PROFEMUR LX REVISION 5/8 COATED HIP STEM

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