PMA P010015S473

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
S473
Product code
LWP
Decision date
2021-05-18
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Approval order statement
Acceptance to implement a new degreasing process at their component suppliers.

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
S473
Product code
LWP
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Decision date
2021-05-18
Decision code
OK30
Date received
2021-04-20
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Acceptance to implement a new degreasing process at their component suppliers.