PMA P970020S084
- Device
- MULTI-LINK ULTRA RX Coronary Stent System
- Applicant
- Abbott Vascular, Inc.
- PMA number
- P970020
- Supplement
- S084
- Product code
- MAF
- Decision date
- 2019-12-13
- Generic name
- STENT, CORONARY
- Approval order statement
- Change to an alternate supplier for hypotube components.
Current openFDA PMA Record#
- Device
- MULTI-LINK ULTRA RX Coronary Stent System
- Applicant
- Abbott Vascular, Inc.
- PMA number
- P970020
- Supplement
- S084
- Product code
- MAF
- Generic name
- STENT, CORONARY
- Decision date
- 2019-12-13
- Decision code
- OK30
- Date received
- 2019-11-15
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Change to an alternate supplier for hypotube components.