PMA P090013S325
- Device
- CapSureFix MRI Lead
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S325
- Product code
- LWP
- Decision date
- 2022-11-22
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- Relocation of the Chemical Operations area within the same manufacturing facility (Medtronic Energy and Component Center) for selected components.
Current openFDA PMA Record#
- Device
- CapSureFix MRI Lead
- Applicant
- Medtronic, Inc.
- PMA number
- P090013
- Supplement
- S325
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 2022-11-22
- Decision code
- OK30
- Date received
- 2022-11-16
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Relocation of the Chemical Operations area within the same manufacturing facility (Medtronic Energy and Component Center) for selected components.