FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Affinity Fusion Oxygenator System, Affinity Pixie Oxygenation System

K Number: K203111 · Decision Sep 16, 2021
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
253
Applicant Total
33
Review Days
336

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Basic Information

Device Name
Affinity Fusion Oxygenator System, Affinity Pixie Oxygenation System
K Number
K203111
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic
Date Received
October 15, 2020
Decision Date
September 16, 2021
Product Code
DTZ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTZ Oxygenator, Cardiopulmonary Bypass

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K240190 MYOtherm XP Cardioplegia Delivery System with Cortiva BioActive Surface, MYOtherm XP Cardioplegia Delivery System Uncoated
K223494 CD Horizon Spinal System
K223178 SelectSite C304 Deflectable Catheter System, C315 Delivery System
K222873 Attain Command + SureValve Delivery System, Attain Select II + SureValve delivery system
K221244 CD Horizon™ Spinal System
K211596 CD Horizon Spinal System
K210637 CD Horizon™ Spinal System
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