K-number	K090303
Device name	XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004
Applicant	Corespine Technologies, LLC
Product code	HRX
Device class	Class II
Decision date	Apr 30, 2009
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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XTEND-ST NUCLEUS REMOVAL SYSTEM, MODEL 9004

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