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ENDURANT STENT GRAFT SYSTEM, ENDURANT (II/IIS) STENT GRAFT SYSTEM, ENDURANT II AORTO-UNI-ILIAC (AUI) STENT GRAFT SYSTEM

FDA premarket approval P100021/S045 · decided 2015-03-25

Approval details

PMA number
P100021
Supplement
S045
Supplement type
Special (Immediate Track)
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ENDURANT STENT GRAFT SYSTEM, ENDURANT (II/IIS) STENT GRAFT SYSTEM, ENDURANT II AORTO-UNI-ILIAC (AUI) STENT GRAFT SYSTEM
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Medtronic Vascular
Date received
2015-02-26
Decision date
2015-03-25
Days to decision
27 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Rosa, CA
Statement
APPROVAL FOR THE ADDITION OF A MANUFACTURING AID TO BE USED DURING THE THUMBWHEEL ASSEMBLY PROCESS.

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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