Atlas FDA

Impella CP with SmartAssist

FDA premarket approval P140003/S122 · decided 2025-02-04

Approval details

PMA number
P140003
Supplement
S122
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Impella CP with SmartAssist
Generic name
Temporary non-roller type left heart support blood pump
Applicant
Abiomed, Inc.
Date received
2024-10-30
Decision date
2025-02-04
Days to decision
97 days
Decision code
APPR
Product code
OZD
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
approval for changes in the design of the Sheath Anchor sub-component of the Integrated Sheath Lock.

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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