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SYNCHROMED INFUSION SYSTEM

FDA premarket approval P860004/S244 · decided 2016-01-08

Approval details

PMA number
P860004
Supplement
S244
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SYNCHROMED INFUSION SYSTEM
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2015-12-11
Decision date
2016-01-08
Days to decision
28 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
CHANGE TO THE INCOMING INSPECTION METHODS FOR COIL INSULATION AND COIL RESISTANCE FOR THE MOTOR USED IN THE SYNCHROMED® II PUMP.

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510(k) clearances by this applicant

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VitalFlow Set with Balance™ Biosurface (K261335)Medtronic, Inc.2026-07-31
Concerto Versa™ Detachable Coil (K261866)Medtronic, Inc.2026-06-24
Elongated One-Piece Arterial (EOPA) 3D™ Arterial Cannulae (K260195)Medtronic, Inc.2026-04-23
Retrograde Coronary Sinus Perfusion Cannulae (K253203)Medtronic, Inc.2026-02-19
Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
Bio-Medicus Life Support Catheter and Introducer (K251831)Medtronic, Inc.2026-01-15
Concerto Versa™ Detachable Coil (K253511)Medtronic, Inc.2026-01-14
C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19