Atlas FDA

Impella RP and Impella RP with SmartAssist

FDA premarket approval P170011/S046 · decided 2022-10-11

Approval details

PMA number
P170011
Supplement
S046
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Impella RP and Impella RP with SmartAssist
Generic name
Temporary non-roller type right heart support blood pump
Applicant
Abiomed, Inc.
Date received
2022-09-15
Decision date
2022-10-11
Days to decision
26 days
Decision code
OK30
Product code
PYX
Advisory committee
Cardiovascular
Expedited review
No
Location
Danvers, MA
Statement
Modification to the process used to construct the retainer within the hybrid bearing of the motor.

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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