K-number	K012551
Device name	LIVERPOOL RADIAL HEAD REPLACEMENT DEVICE
Applicant	Biomet, Inc.
Product code	KWI
Device class	Class II
Decision date	Jan 30, 2002
Decision	Substantially Equivalent
Regulation	888.3170

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View the full FDA submission: accessdata.fda.gov

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LIVERPOOL RADIAL HEAD REPLACEMENT DEVICE

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