K-number	K030048
Device name	HA PMI FEMORAL HIP STEM
Applicant	Biomet Orthopedics, Inc.
Product code	LPH
Device class	Class II
Decision date	Feb 5, 2003
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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HA PMI FEMORAL HIP STEM

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