PMA P010015S577

Device
Percepta Bipolar CRT-P; Perceota Quadrioolar CRT-P; Serena Bipolar CRT-P; Serena Quadripolar CRT-P; Solara Bipolar CRT-P
Applicant
Medtronic, Inc.
PMA number
P010015
Supplement
S577
Product code
LWP
Decision date
2026-01-23
Classification
Cardiovascular
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Approval order statement
implementation for the back half of an additional battery manufacturing line for battery used in Medtronic devices

Current openFDA PMA Record#

Device
Percepta Bipolar CRT-P; Perceota Quadrioolar CRT-P; Serena Bipolar CRT-P; Serena Quadripolar CRT-P; Solara Bipolar CRT-P
Applicant
Medtronic, Inc.
PMA number
P010015
Supplement
S577
Product code
LWP
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Decision date
2026-01-23
Decision code
OK30
Date received
2026-01-12
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
implementation for the back half of an additional battery manufacturing line for battery used in Medtronic devices