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Advisa DR IPG A4DR01 Advisa DR MRI IPG A2DR01 Advisa SR MRI IPG A3SR01 Astra S DR MRI IPG X3DR01 Astra S SR MRI IPG X3SR

FDA premarket approval P980035/S811 · decided 2025-05-30

Approval details

PMA number
P980035
Supplement
S811
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Advisa DR IPG A4DR01 Advisa DR MRI IPG A2DR01 Advisa SR MRI IPG A3SR01 Astra S DR MRI IPG X3DR01 Astra S SR MRI IPG X3SR
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2025-04-30
Decision date
2025-05-30
Days to decision
30 days
Decision code
OK30
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
updates to battery manufacturing including tool modification, eliminating a redundant manufacturing step, and removal of a cleaning agent

Class III intelligence, same tools

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510(k) clearances by this applicant

RecordFirmDate
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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