K-number	K012019
Device name	COLOR BUFFED (CB) DDH FEMORAL STEM
Applicant	Biomet, Inc.
Product code	JDI
Device class	Class II
Decision date	Jul 20, 2001
Decision	Substantially Equivalent
Regulation	888.3350

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View the full FDA submission: accessdata.fda.gov

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COLOR BUFFED (CB) DDH FEMORAL STEM

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