PMA P090013S135
- Device
- REVO MRI IPG
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S135
- Product code
- LWP
- Decision date
- 2014-04-04
- Classification
- Implantable Pulse Generator, Pacemaker (non-crt)
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- MANUFACTURING PROCESS CHANGE FOR THE PRINTED WIRING BOARD (PWB) SUBSTRATES AT A MEDTRONIC SECOND TIER SUPPLIER. THESE PWB SUBSTRATES ARE USED IN THE MANUFACTURE OF HYBRID SUBSTRATES AT MEDTRONIC¿S INTERNAL SUPPLIER, MEDTRONIC TEMPE CAMPUS (MTC), FOR THE DEVICES.
Current openFDA PMA Record#
- Device
- REVO MRI IPG
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S135
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 2014-04-04
- Decision code
- OK30
- Date received
- 2014-03-07
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- MANUFACTURING PROCESS CHANGE FOR THE PRINTED WIRING BOARD (PWB) SUBSTRATES AT A MEDTRONIC SECOND TIER SUPPLIER. THESE PWB SUBSTRATES ARE USED IN THE MANUFACTURE OF HYBRID SUBSTRATES AT MEDTRONIC¿S INTERNAL SUPPLIER, MEDTRONIC TEMPE CAMPUS (MTC), FOR THE DEVICES.