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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