Atlas FDA

CapSureFix Novus Lead

FDA premarket approval P930039/S269 · decided 2025-02-20

Approval details

PMA number
P930039
Supplement
S269
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CapSureFix Novus Lead
Generic name
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes
Applicant
Medtronic, Inc.
Date received
2025-01-28
Decision date
2025-02-20
Days to decision
23 days
Decision code
OK30
Product code
NVN
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
adding an additional ethylene oxide sterilization system at Medtronic Singapore Operations

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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