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Consulta CRT-P C4TR01 Percepta Bipolar CRT-P W1TR01 Percepta Quadripolar CRT-P W4TR01 Serena Bipolar CRTP W1TR02 Serena

FDA premarket approval P010015/S561 · decided 2025-04-25

Approval details

PMA number
P010015
Supplement
S561
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Consulta CRT-P C4TR01 Percepta Bipolar CRT-P W1TR01 Percepta Quadripolar CRT-P W4TR01 Serena Bipolar CRTP W1TR02 Serena
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Medtronic, Inc.
Date received
2025-03-20
Decision date
2025-04-25
Days to decision
36 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
manufacturing changes to the dielectric formation process for TBC style tantalum capacitor components

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