Atlas FDA

CapSureFix Novus Lead

FDA premarket approval P930039/S221 · decided 2020-12-10

Approval details

PMA number
P930039
Supplement
S221
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
2020-12-07
Decision date
2020-12-10
Days to decision
3 days
Decision code
OK30
Product code
NVN
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Update the FACTORYworks Web User Interface to version 1.1.0.

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510(k) clearances by this applicant

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Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
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C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409)Medtronic, Inc.2025-12-19