Affinity CP Centrifugal Blood Pump, Affinity CP Centrifugal Blood Pump with Balance Biosurface, Affinity CP Centrifugal Blood Pump with Cortiva BioActive Surface

FDA 510(k) K201068 · Medtronic, Inc.

Substantially Equivalent

510(k) numberK201068

Submission

Device name
Affinity CP Centrifugal Blood Pump, Affinity CP Centrifugal Blood Pump with Balance Biosurface, Affinity CP Centrifugal Blood Pump with Cortiva BioActive Surface
Applicant
Medtronic, Inc.
Minneapolis, MN, US
Received
April 22, 2020
Decision date
May 21, 2020
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KFM – Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4360
Specialty
Cardiovascular

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K250326Quantum Perfusion Centrifugal Blood Pump CP22NG with Integrated Sensors (CP22V-NG)KFM · Traditional Spectrum Medical S.R.L.06/24/2025SE
K233091Quantum Perfusion Centrifugal Blood Pump CP37 with Integrated Sensors (CP37V-VT)…KFM · Special Qura S.R.L10/26/2023SE
K232132LifeSPARC SystemKFM · Special Cardiacassist, Inc.08/03/2023SE
K220842Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors, Quantum Perfusion…KFM · Traditional Qura S.R.L05/19/2023SE
K200091Capiox iCP Centrifugal PumpKFM · Traditional Terumo Cardiovascular Systems Corporation11/18/2021SE
K201320Quantum PureFlow Centrifugal Blood Pump CP22 with Integrated SensorKFM · Traditional Qura S.R.L11/03/2021SE
K193663FloPump 57mL Centrifugal PumpKFM · Traditional International Biophysics Corporation03/10/2021SE
K202169Quantum PureFlow Centrifugal Blood Pump CP37, Quantum PureFlow Centrifugal Blood Pump CP22KFM · Special Qura S.R.L09/02/2020SE
K192850Quantum PureFlow Centrifugal Blood Pump CP37, Quantum PureFlow Centrifugal Blood Pump CP22KFM · Traditional Qura S.R.L04/13/2020SE

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Questions and answers

When was Affinity CP Centrifugal Blood Pump, Affinity CP Centrifugal Blood Pump with Balance Biosurface, Affinity CP Centrifugal Blood Pump with Cortiva BioActive Surface cleared by the FDA?

Affinity CP Centrifugal Blood Pump, Affinity CP Centrifugal Blood Pump with Balance Biosurface, Affinity CP Centrifugal Blood Pump with Cortiva BioActive Surface (K201068) received a 510(k) decision of Substantially Equivalent on May 21, 2020, 29 days after the submission was received.

What is the product code of K201068?

The FDA product code is KFM – Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type, a Class II (moderate risk) device regulated under 21 CFR 870.4360.