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OMNILINK ELITE VASCULAR BALLOON-EXPANDABLE STENT SYSTEM

FDA premarket approval P110043/S001 · decided 2012-09-07

Approval details

PMA number
P110043
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
OMNILINK ELITE VASCULAR BALLOON-EXPANDABLE STENT SYSTEM
Generic name
STENT, ILIAC
Applicant
Abbott Vascular-Cardiac Therapies
Date received
2012-08-24
Decision date
2012-09-07
Days to decision
14 days
Decision code
OK30
Product code
NIO
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Clara, CA
Statement
NEW STRAIGHTNESS TEST FOR COBALT CHROMIUM STENT TUBING.

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510(k) clearances by this applicant

RecordFirmDate
HI-TORQUE POWERTURN (K112957)Abbott Vascular-Cardiac Therapies2011-11-08
NC TREK RX CORONARY DILATATION CATHETER (K110134)Abbott Vascular-Cardiac Therapies2011-02-11
HI-TORQUE BALANCE MIDDLEWEIGHT ELITE (K103101)Abbott Vascular-Cardiac Therapies2011-02-10
MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER (K103110)Abbott Vascular-Cardiac Therapies2011-01-10
VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETER (K103153)Abbott Vascular-Cardiac Therapies2010-12-30
HI-TORQUE PILOT 50 AND 150 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER LS AND MS GUIDE WIRE WITH (K101116)Abbott Vascular-Cardiac Therapies2010-06-23