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Impella 2.5, Impella CP, Impella CP with SmartAssist, Impella 5.0, and Impella 5.5 with SmartAssist Systems

FDA premarket approval P140003/S117 · decided 2023-12-21

Approval details

PMA number
P140003
Supplement
S117
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Impella 2.5, Impella CP, Impella CP with SmartAssist, Impella 5.0, and Impella 5.5 with SmartAssist Systems
Generic name
Temporary non-roller type left heart support blood pump
Applicant
Abiomed, Inc.
Date received
2023-12-18
Decision date
2023-12-21
Days to decision
3 days
Decision code
APPR
Product code
OZD
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
approval for changes to the device labeling for the continued safe use of Impella catheters in regard to ventricular perforation and cotton fiber ingestion.

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510(k) clearances by this applicant

RecordFirmDate
14Fr Low Profile Introducer Kit (K252766)Abiomed, Inc.2025-10-08
Abiomed 14Fr Low Profile Introducer Kit (K241708)Abiomed, Inc.2024-08-06
preCARDIA Occlusion System (K221294)Abiomed, Inc.2023-06-30
OXY-1 System (K223161)Abiomed, Inc.2023-02-23
Abiomed 14Fr Low Profile Introducer Set (K222113)Abiomed, Inc.2022-10-13
Impella XR Sheath Set (K202330)Abiomed, Inc.2020-12-07
OXY-1 System (K200109)Abiomed, Inc.2020-10-23
Abiomed 23 Fr Sheath (K201116)Abiomed, Inc.2020-06-15