K-number	K030971
Device name	MODIFICATION TO MODULAR PLUS REVISION STEM
Applicant	Plus Orthopedics
Product code	LWJ
Device class	Class II
Decision date	Apr 24, 2003
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO MODULAR PLUS REVISION STEM

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