K-number	K061698
Device name	MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR
Applicant	Life Spine
Product code	JDK
Device class	Class II
Decision date	Jul 12, 2006
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR

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