K-number	K031693
Device name	MALLORY/HEAD MODULAR CALCAR WITH AND WITHOUT HA
Applicant	Biomet, Inc.
Product code	LPH
Device class	Class II
Decision date	Aug 6, 2003
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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MALLORY/HEAD MODULAR CALCAR WITH AND WITHOUT HA

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