K-number	K032034
Device name	ANS AXXESS PERCUTANEOUS LEAD
Applicant	Advanced Neuromodulation Systems
Product code	GZB
Device class	Class II
Decision date	Oct 3, 2003
Decision	Substantially Equivalent
Regulation	882.5880

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View the full FDA submission: accessdata.fda.gov

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ANS AXXESS PERCUTANEOUS LEAD

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