Atlas FDA

LimFlow System

FDA premarket approval P220025 · decided 2023-09-11

Approval details

PMA number
P220025
Trade name
LimFlow System
Generic name
Stent graft, infrapopliteal, venous arterialization
Applicant
LimFlow, Inc.
Date received
2022-10-31
Decision date
2023-09-11
Days to decision
315 days
Decision code
APPR
Product code
QWN
Advisory committee
Cardiovascular
Expedited review
No
Location
San Jose, CA
Statement
Approval for The LimFlow System. The device is indicated for patients who have chronic limb-threatening ischemia with no suitable endovascular or surgical revascularization options and are at risk of major amputation.

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510(k) clearances by this applicant

RecordFirmDate
LimFlow Vector (K260188)LimFlow, Inc.2026-03-18
LimFlow ARC (K251376)LimFlow, Inc.2025-05-31
LimFlow V-Ceiver (K242776)LimFlow, Inc.2025-02-14
LimFlow Vector (K221902)LimFlow, Inc.2022-12-21
LimFlow ARC (K221541)LimFlow, Inc.2022-08-31
LimFlow V-Ceiver (K222083)LimFlow, Inc.2022-08-09