Atlas FDA

VALIANT THORACIC STENT GRAFT WITH THE CAPTIVIA DELIVERY SYSTEM

FDA premarket approval P100040/S003 · decided 2011-05-25

Approval details

PMA number
P100040
Supplement
S003
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VALIANT THORACIC STENT GRAFT WITH THE CAPTIVIA DELIVERY SYSTEM
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Medtronic Vascular
Date received
2011-04-26
Decision date
2011-05-25
Days to decision
29 days
Decision code
OK30
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Rosa, CA
Statement
TRANSFER OF POST STERILIZATION INSPECTIONS TO AN ALTERNATE SITE.

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
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