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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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