K-number	K051371
Device name	INTERBODY INNOVATIONS CEMENT RESTRICTOR
Applicant	Interbody Innovations, Llp
Product code	JDK
Device class	Class II
Decision date	Dec 6, 2005
Decision	Unknown
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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INTERBODY INNOVATIONS CEMENT RESTRICTOR

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