PMA P010015S496

Device
Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Sola
Applicant
Medtronic, Inc.
PMA number
P010015
Supplement
S496
Product code
LWP
Decision date
2022-04-26
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Approval order statement
Implement minor updates in the manufacturing of hybrids at Medtronic Tempe Campus.

Current openFDA PMA Record#

Device
Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Sola
Applicant
Medtronic, Inc.
PMA number
P010015
Supplement
S496
Product code
LWP
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Decision date
2022-04-26
Decision code
OK30
Date received
2022-04-22
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Implement minor updates in the manufacturing of hybrids at Medtronic Tempe Campus.