FDA 510(k) Applications Submitted by PENNY HOUSTON

FDA 510(k) Number Submission Date Device Name Applicant
K070847 03/28/2007 TRIAL CABLE, 3009 ADVANCED NEUROMODULATION SYSTEMS
K081208 04/29/2008 CINCH ANCHOR, MODEL 1194 ADVANCED NEUROMODULATION SYSTEMS
K112214 08/02/2011 OCTRODEX(TM), QUATTRODEX(TM), INTRODEX(TM), EPIDURAL NEEDLE, STYLETS ST. JUDE MEDICAL NEUROMODULATION
K092371 08/05/2009 SWIFT-LOCK ANCHOR, MODEL 1192 ADVANCED NEUROMODULATION SYSTEMS


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