Atlas FDA

Pipeline Vantage Embolization Device with Shield Technology

FDA premarket approval P100018/S034 · decided 2023-09-15

Approval details

PMA number
P100018
Supplement
S034
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Pipeline Vantage Embolization Device with Shield Technology
Generic name
Intracranial aneurysm flow diverter
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
Date received
2021-09-27
Decision date
2023-09-15
Days to decision
718 days
Decision code
APPR
Product code
OUT
Advisory committee
Neurology
Expedited review
No
Location
Irvine, CA
Statement
Approval for a new neurovascular flow-diverting stent and delivery system in the Pipeline product family.

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510(k) clearances by this applicant

RecordFirmDate
Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter (K241388)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2025-01-02
Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing (K243418)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-12-02
Riptide Aspiration System (K243080)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2024-10-29
Rist 071 Radial Access Guide Catheter (K211990)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2021-07-27
Axium Detachable Coil; Axium Prime Detachable Coil (K203432)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2021-07-07
Solitaire X Revascularization Device (K203358)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2021-03-01
Concerto Versa, Detachable Coil (K202850)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2021-02-09
Solitaire Platinum Revascularization Device, Solitaire X Revascularization Device (Solitaire Revascularization Device) (K193576)Micro Therapeutics, Inc. d/b/a ev3 Neurovascular2020-11-20