K-number	K051363
Device name	RESTORATION MODULAR SYSTEM
Applicant	Howmedica Osteonics Corp.
Product code	JDI
Device class	Class II
Decision date	Jun 23, 2005
Decision	Substantially Equivalent
Regulation	888.3350

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Source

View the full FDA submission: accessdata.fda.gov

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RESTORATION MODULAR SYSTEM

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