PMA P130021S086

Device
CoreValve EnVeo R Delivery Catheter System, CoreValve EnVeo R Loading System, CoreValve EnVeo Proo Delivery Catheter Sys
Applicant
Medtronic, Inc.
PMA number
P130021
Supplement
S086
Product code
NPT
Decision date
2021-03-02
Generic name
Aortic valve, prosthesis, percutaneously delivered
Approval order statement
Use of an electronic Manufacturing Execution System (MES) to replace the current paper-based device history record (DHR).

Current openFDA PMA Record#

Device
CoreValve EnVeo R Delivery Catheter System, CoreValve EnVeo R Loading System, CoreValve EnVeo Proo Delivery Catheter Sys
Applicant
Medtronic, Inc.
PMA number
P130021
Supplement
S086
Product code
NPT
Generic name
Aortic valve, prosthesis, percutaneously delivered
Decision date
2021-03-02
Decision code
OK30
Date received
2021-02-25
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Use of an electronic Manufacturing Execution System (MES) to replace the current paper-based device history record (DHR).