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XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM, SV

FDA premarket approval P110019/S047 · decided 2014-04-23

Approval details

PMA number
P110019
Supplement
S047
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM, SV
Generic name
Coronary drug-eluting stent
Applicant
Abbott Vascular
Date received
2013-05-22
Decision date
2014-04-23
Days to decision
336 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Clara, CA
Statement
APPROVAL FOR AN UPDATE TO THE LABELING FOR THE XIENCE XPEDITION RX (RAPID EXCHANGE) AND OTW (OVER-THE-WIRE) TO CHANGE THE GUIDING CATHETER COMPATIBILITY FOR THE 4.0MM BALLOON DIAMETER SIZES FROM A MINIMUM OF A 6 FRENCH (F) GUIDE CATHETER TO 5F FOR THE 4.0 X 8-33MM SIZES.

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510(k) clearances by this applicant

RecordFirmDate
NC TREK NEO Coronary Dilatation Catheter (K220634)Abbott Vascular2022-06-30
Viatrac 14 Plus Peripheral Dilatation Catheter (K221057)Abbott Vascular2022-05-05
HI-TORQUE PROCEED Guide Wire Family (K201834)Abbott Vascular2020-07-30
HI-TORQUE Steelcore Bare Guide Wire (K200144)Abbott Vascular2020-04-08
HI-TORQUE InfilTrac Guide Wire Family (K193126)Abbott Vascular2019-12-11
Emboshield NAV6 Embolic Protection System, Barewire Filter Delivery Wires (K191173)Abbott Vascular2019-07-25
NC TREK™ RX Coronary Dilatation Catheter; NC TREK™ OTW Coronary Dilatation Catheter; TREK™ RX Coronary Dilatation Catheter; TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ RX Coronary Dilatation Catheter; MINI TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ II OTW Coronary Dilatation Catheter (K180040)Abbott Vascular2018-08-24
HI-TORQUE TurnTrac Guide Wire Family (K173795)Abbott Vascular2018-01-12