K-number	K082991
Device name	BIOLOX DELTA CERAMIC FEMORAL HEAD
Applicant	Aesculap Implant Systems, Inc.
Product code	LZO
Device class	Class II
Decision date	Nov 20, 2008
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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BIOLOX DELTA CERAMIC FEMORAL HEAD

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