Atlas FDA

Myocardial Pacing Lead

FDA premarket approval P120017/S037 · decided 2024-11-13

Approval details

PMA number
P120017
Supplement
S037
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Myocardial Pacing Lead
Generic name
permanent pacemaker Electrode
Applicant
Medtronic, Inc.
Date received
2024-10-17
Decision date
2024-11-13
Days to decision
27 days
Decision code
OK30
Product code
DTB
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
to update the manufacturing execution system to FACTORYworks Release 10.0

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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