K-number	K070369
Device name	REGENERX RINGLOC + MODULAR ACETABULAR SHELLS
Applicant	Biomet, Inc.
Product code	LPH
Device class	Class II
Decision date	Mar 9, 2007
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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REGENERX RINGLOC + MODULAR ACETABULAR SHELLS

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