K-number	K022615
Device name	CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR
Applicant	Centerpulse Spine-Tech, Inc.
Product code	JDK
Device class	Class II
Decision date	Oct 29, 2002
Decision	Unknown
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

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