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Impella 2.5, Impella CP, Impella CP with SmartAssist, Impella 5.0, Impella LD

FDA premarket approval P140003/S044 · decided 2019-04-17

Approval details

PMA number
P140003
Supplement
S044
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Impella 2.5, Impella CP, Impella CP with SmartAssist, Impella 5.0, Impella LD
Generic name
Temporary non-roller type left heart support blood pump
Applicant
Abiomed, Inc.
Date received
2018-12-26
Decision date
2019-04-17
Days to decision
112 days
Decision code
APPR
Product code
OZD
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
Approval for modifications to the Instructions for Use (IFU) to add the option to use either bivalirudin or argatroban to achieve the recommended level of systemic anticoagulation for Impella patients.

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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