PMA P930022

Device
Legend Plus Ipg
Applicant
MEDTRONIC Inc.
PMA number
P930022
Supplement
S017
Decision date
2015-10-19

Current openFDA PMA Record

Device
Medtronic(R) Legend Plus(TM) Pulse Generator
Applicant
Medtronic, Inc.
PMA number
P930022
Supplement
S020
Product code
NVZ
Generic name
Pulse generator, permanent, implantable
Decision date
2025-03-20
Decision code
APPR
Date received
2025-02-13
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
approval for a predetermined change control plan (PCCP) that encompasses the following biocompatibility-related manufacturing changes, provided that they do not impact the properties of the device materials, for the devices under the above PMAs:1. Removal of a processing aid (solvent, lubricant, antifoaming agent, etc.), or cleaning agent2. Removal of a cleaning process3. Change in parameters (temperature, time, sonication, etc.) of a current cleaning process

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