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IMPLANTABLE INFUSION SYSTEM

FDA premarket approval P860004/S162 · decided 2011-12-12

Approval details

PMA number
P860004
Supplement
S162
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
IMPLANTABLE INFUSION SYSTEM
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2011-11-04
Decision date
2011-12-12
Days to decision
38 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
RELOCATION OF PASSIVATION OPERATIONS AND INTRODUCTION OF AN AUTOMATED FLUID TRANSFER PROCESS WITHIN THE EXISTING MEDTRONIC NEUROMODULATION FACILITY ¿ RICE CREEK CENTRAL.

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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