Atlas FDA

MULTI-LINK VISION CORONARY STENT SYSTEMS

FDA premarket approval P020047/S008 · decided 2007-02-16

Approval details

PMA number
P020047
Supplement
S008
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MULTI-LINK VISION CORONARY STENT SYSTEMS
Generic name
STENT, CORONARY
Applicant
Abbott Vascular
Date received
2007-01-19
Decision date
2007-02-16
Days to decision
28 days
Decision code
OK30
Product code
MAF
Advisory committee
Cardiovascular
Expedited review
No
Location
Temecula, CA
Statement
MODIFICATION IN THE DOSE RANGE AND CONVEYOR SPEED FOR E-BEAM STERILIZATION FOR THE MULTI-LINK AND MULTI-LINK VISION CORONARY STENT SYSTEMS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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