K-number	K053588
Device name	PROFEMUR LX HIP STEM
Applicant	Wrightmedicaltechnologyinc
Product code	KWA
Device class	Class III
Decision date	Jan 13, 2006
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 HIP STEM

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