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FDA 510(k) Applications Submitted by EV3 CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K031864
06/16/2003
NITREX NITINOL GUIDEWIRE
EV3 CORPORATION
K050725
03/21/2005
PROTEGE GPS SELF-EXPANDING NITINOL STENT
EV3 CORPORATION
K051379
05/27/2005
PROTEGE RX GPS SELF-EXPANDING NITRINOL STENT
EV3 CORPORATION
K021096
04/04/2002
X-SIZER CATHETER SYSTEM
EV3 CORPORATION
K024021
12/05/2002
NITREX NITINOL GUIDEWIRE
EV3 CORPORATION
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