PMA P870021S001
- Device
- PRIME{TM} MODEL 6520, 6525, 6530 AND 6535
- Applicant
- Medtronic, Inc.
- PMA number
- P870021
- Supplement
- S001
- Product code
- LOX
- Decision date
- 1988-10-13
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
Current openFDA PMA Record
- Device
- PRIME{TM} MODEL 6520, 6525, 6530 AND 6535
- Applicant
- Medtronic, Inc.
- PMA number
- P870021
- Supplement
- S001
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1988-10-13
- Decision code
- APPR
- Date received
- 1988-03-28
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material