K-number	K062997
Device name	ARCOMXL POLYETHYLENE LINERS AND 38/40MM FEMORAL HEADS
Applicant	Biomet Manufacturing Corp
Product code	LZO
Device class	Class II
Decision date	Dec 8, 2006
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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ARCOMXL POLYETHYLENE LINERS AND 38/40MM FEMORAL HEADS

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