FDA 510(k) Applications Submitted by SUSAN WALTON

FDA 510(k) Number Submission Date Device Name Applicant
K130050 01/09/2013 TITAN REVERSE SHOULDER SYSTEM ASCENSION ORTHOPEDIC
K000744 03/07/2000 MEDTRONIC AVE BRIDGE X3 STENT MEDTRONIC AVE, INC.
K110700 03/14/2011 ASCENSION ATLAS HUMERAL PLATING SYSTEM ASCENSION ORTHOPEDICS, INC.
K991533 05/03/1999 MEDTRONIC AVE STENT DELIVERY SYSTEM - FOR USE IN BILIARY INDICATION PERIPHERAL AVE
K121826 06/21/2012 INTEGRA PROXIMAL HUMERAL PLATE SYSTEM ASCENSION ORTHOPEDICS, INC.
K992318 07/12/1999 MEDTRONIC AVE BRIDGE STENT MEDTRONIC AVE, INC.
K992569 08/02/1999 MEDTRONIC AVE BRIDGE STENT MEDTRONIC AVE, INC.
K112438 08/24/2011 TITAN MODULAR TOTAL SHOULDER SYSTEM ASCENSION ORTHOPEDIC
K102549 09/07/2010 THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY ASCENSION ORTHOPEDICS, INC.
K993145 09/20/1999 MEDTRONIC AVE BRIDGE STENT MEDTRONIC AVE, INC.
K964612 11/18/1996 VISTAKON (GENFILCON A) CONTACT LENS, CLEAR AND WITH VISIBILIITY TINT VISTAKON, JOHNSON & JOHNSON VISION PRODUCTS, INC.


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