FDA 510(k) Applications Submitted by DAVID PADGETT

FDA 510(k) Number Submission Date Device Name Applicant
K090060 01/09/2009 NEXLINK OCT SYSTEM, MODEL 7000 SERIES ABBOTT SPINE, INC.
K121671 06/06/2012 PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM ZIMMER SPINE, INC.
K082032 07/17/2008 SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310) ABBOTT SPINE, INC.
K072672 09/21/2007 SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES ABBOTT SPINE, INC.
K100845 03/25/2010 PATHFINDER II, MINIMALLY INVASIE PEDICLE SCREW SYSTEM MODEL 3500 SERIES ZIMMER SPINE, INC


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