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OMNILINK ELITE PERIPHERAL BALLOON-EXPANDABLE STENT SYSTEM

FDA premarket approval P110043 · decided 2012-07-31

Approval details

PMA number
P110043
Trade name
OMNILINK ELITE PERIPHERAL BALLOON-EXPANDABLE STENT SYSTEM
Generic name
STENT, ILIAC
Applicant
Abbott Vascular-Cardiac Therapies
Date received
2011-12-30
Decision date
2012-07-31
Days to decision
214 days
Decision code
APPR
Product code
NIO
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Clara, CA
Statement
APPROVAL FOR THE OMNILINK ELITE VASCULAR BALLOON-EXPANDABLE STENT SYSTEM. THIS DEVICE IS INDICATED FOR THE TREATMENT OF ATHEROSCLEROTIC ILIAC ARTERY LESIONS WITH REFERENCE VESSEL DIAMETERS OF >= 5.0 MM AND <= 11.0 MM AND LESION LENGTHS UP TO 50 MM.

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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