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Percepta Bipolar CRT-P, Percepta Quadripolar CR T-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Solara Bipolar CRT-

FDA premarket approval P010015/S540 · decided 2024-05-29

Approval details

PMA number
P010015
Supplement
S540
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Percepta Bipolar CRT-P, Percepta Quadripolar CR T-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Solara Bipolar CRT-
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Medtronic, Inc.
Date received
2024-05-15
Decision date
2024-05-29
Days to decision
14 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
to update the stack insertion step in the connector module manufacturing process at MECC

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