K-number	K042953
Device name	MODIFICATION TO PROTEX STABILIZATION SYSTEM
Applicant	Globus Medical, Inc.
Product code	NKB
Device class	Class II
Decision date	Nov 22, 2004
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO PROTEX STABILIZATION SYSTEM

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