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Resolute Integrity Rapid Exchange Coronary Stent System

FDA premarket approval P110013/S103 · decided 2020-10-05

Approval details

PMA number
P110013
Supplement
S103
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Resolute Integrity Rapid Exchange Coronary Stent System
Generic name
Coronary drug-eluting stent
Applicant
Medtronic Vascular
Date received
2020-07-10
Decision date
2020-10-05
Days to decision
87 days
Decision code
APPR
Product code
NIQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Rosa, CA
Statement
Approval for site change for packaging and labeling rework processes.

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510(k) clearances by this applicant

RecordFirmDate
Steerantâ„¢ Super Stiff Guidewire (K232570)Medtronic Vascular2023-10-24
6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter (K232190)Medtronic Vascular2023-08-22
5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter (K230156)Medtronic Vascular2023-06-30
Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P) (K220773)Medtronic Vascular2022-04-13
Medtronic 6F Taiga Guiding Catheter (K192296)Medtronic Vascular2019-09-20
Admiral Xtreme (K173515)Medtronic Vascular2018-04-12
InTRAkit (K162097)Medtronic Vascular2016-11-17
TRAcelet Compression Device (K162027)Medtronic Vascular2016-10-21