FDA 510(k) Applications Submitted by ST. JUDE MEDICAL NEUROMODULATION

FDA 510(k) Number Submission Date Device Name Applicant
K112214 08/02/2011 OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS ST. JUDE MEDICAL NEUROMODULATION
K123299 10/23/2012 MTS SYSTEM, WIDE-SPACE QUATTRODE PERCUTANEOUS LEADS ST. JUDE MEDICAL NEUROMODULATION


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