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XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA premarket approval P070015/S122 · decided 2014-10-03

Approval details

PMA number
P070015
Supplement
S122
Supplement type
Panel Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
Generic name
Coronary drug-eluting stent
Applicant
Abbott Vascular, Inc.
Date received
2014-03-21
Decision date
2014-10-03
Days to decision
196 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Temecula, CA
Statement
APPROVAL FOR THE EXPANSION OF THE INDICATIONS FOR USE OF THE XIENCE V AND XIENCE NANO EVEROLIMUS ELUTING CORONARY STENT SYSTEM XIENCE PRIME AND XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM, XIENCE XPEDITION, XIENCE XPEDITION SV AND XIENCE XPEDITION LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM, AND XIENCE ALPINE EVEROLIMUS ELUTING CORONARY STENT SYSTEM TO INCLUDE DE NOVO TOTAL CORONARY OCCLUSIONS.. THESE DEVICES ARE INDICATED FOR THE FOLLOWING:XIENCE V AND XIENCE NANO EVEROLIMUS ELUTIN

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510(k) clearances by this applicant

RecordFirmDate
Hi-Torque JET Guide Wire Family (K142415)Abbott Vascular, Inc.2014-12-19
PROGRESS GUIDE WIRE FAMILY, PILOT GUIDE WIRE FAMILY (K123067)Abbott Vascular, Inc.2013-01-29
HI-TORQUE COMMAND GUIDE WIRE FAMILY (K122573)Abbott Vascular, Inc.2012-11-20
ARMADA 14 PTA CATHETER (K102705)Abbott Vascular, Inc.2010-12-07
HI-TORQUE WINN GUIDE WIRE FAMILY (K101648)Abbott Vascular, Inc.2010-07-08
HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL (K101011)Abbott Vascular, Inc.2010-05-24
HI-TORQUE PROGRESS GUIDE WIRE FAMILY (K091825)Abbott Vascular, Inc.2009-09-25
FOXCROSS PTA CATHETER (K081417)Abbott Vascular, Inc.2008-06-04