K-number	K032396
Device name	RINGLOC 36MM LINE AND MODULAR FEMORAL HEADS
Applicant	Biomet, Inc.
Product code	JDI
Device class	Class II
Decision date	Aug 21, 2003
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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RINGLOC 36MM LINE AND MODULAR FEMORAL HEADS

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