K-number	K063279
Device name	NOVATION SPLINED RDD FEMORAL STEMS
Applicant	Exactech, Inc.
Product code	LZO
Device class	Class II
Decision date	Nov 29, 2006
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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NOVATION SPLINED RDD FEMORAL STEMS

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