Atlas FDA

USCI GRUNTZIG DILACA CATHETER

FDA premarket approval P790017/S017 · decided 1988-03-18

Approval details

PMA number
P790017
Supplement
S017
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
USCI GRUNTZIG DILACA CATHETER
Generic name
Catheters, transluminal coronary angioplasty, percutaneous
Applicant
Medtronic, Ireland
Date received
1987-11-18
Decision date
1988-03-18
Days to decision
121 days
Decision code
APPR
Product code
LOX
Advisory committee
Cardiovascular
Expedited review
No
Location
Galway

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
Euphora Rapid Exchange (RX) Balloon Dilatation Catheter (K261759)Medtronic Ireland2026-07-27
Sprinter Legend Rapid Exchange Balloon Dilatation Catheter (K251970)Medtronic, Ireland2026-01-17
Telescope Guide Extension Catheter (K252390)Medtronic, Ireland2025-10-29
Liberant Thrombectomy System (K250787)Medtronic, Ireland2025-06-11
ATTAIN COMMAND+SUREVALVE LEFT HEART DELIVERY SYSTEM ATTAIN COMMAND GUIDE CATHETERS FOR LEFT HEART DELIVERY,ATTAIN SELECT (K123153)Medtronic, Ireland2013-04-09
SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON (K103095)Medtronic, Ireland2010-10-22
ATTAIN 6227DEF DEFLECTABLE CATHETER DELIVERY SYSTEM (K061480)Medtronic, Ireland2006-08-21
ATTAIN SELECT II 6248DEL DELIVERY CATHETER SYSTEM (K053431)Medtronic, Ireland2006-03-16