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Impella 2.5, Impella CP and CP with SmartAssist

FDA premarket approval P140003/S110 · decided 2023-04-27

Approval details

PMA number
P140003
Supplement
S110
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Impella 2.5, Impella CP and CP with SmartAssist
Generic name
Temporary non-roller type left heart support blood pump
Applicant
Abiomed, Inc.
Date received
2023-03-28
Decision date
2023-04-27
Days to decision
30 days
Decision code
APPR
Product code
OZD
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
Approval of the revised protocol for the Impella Real-World Surveillance of patients using Sodium Bicarbonate. The PAS protocol has been submitted to comply with the conditions of approval outlined in our approval orders for P140003/S088 and P170011/S035.

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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