K-number	K060132
Device name	SPINAL USA CEMENT RESTRICTOR SYSTEM
Applicant	Spinal USA
Product code	JDK
Device class	Class II
Decision date	Mar 16, 2006
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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SPINAL USA CEMENT RESTRICTOR SYSTEM

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