510(k) K033468

AFFINITY 20U ARTERIAL FILTER WITH TRILLIUM BIOSURFACE by Medtronic Perfusion Systems — Product Code DTM

K033468 is an FDA 510(k) premarket notification submitted by Medtronic Perfusion Systems for the device "AFFINITY 20U ARTERIAL FILTER WITH TRILLIUM BIOSURFACE". The FDA issued a decision of Substantially Equivalent on November 14, 2003. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Medtronic Perfusion Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 2003
Date Received
November 3, 2003
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class
Class II
Regulation Number
870.4260
Review Panel
CV
Submission Type