K-number	K072537
Device name	CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM
Applicant	Creaspine Sas
Product code	MQP
Device class	Class II
Decision date	Dec 18, 2007
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM

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