Atlas FDA

SYNCHROMED PUMP AND INFUSION SYSTEM

FDA premarket approval P860004/S191 · decided 2013-05-23

Approval details

PMA number
P860004
Supplement
S191
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
SYNCHROMED PUMP AND INFUSION SYSTEM
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2013-04-25
Decision date
2013-05-23
Days to decision
28 days
Decision code
APPR
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
APPROVAL OF LABELING CHANGES FOR DEVICE REFILL KIT MODEL 8551 TO ACCOMMODATE THE POSSIBILITY FOR THE USE OF MULTIPLE SYRINGES DURING KIT REFILL PROCEDURES.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
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