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AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACE

K123351 Class II Traditional
Decision Date
2013-03-19
Sponsor / Applicant
Medtronic Perfusion Systems

Technical Specification

510(k) Submission ID K123351
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 2013-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACE received FDA 510(k) clearance under submission number K123351, sponsored by Medtronic Perfusion Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code DTM and 21 CFR 870.4260, within the Cardiovascular review panel as a Class II device.