PMA P160043S010
- Device
- Resolute Onyx Zotarolimus-Eluting Coronary Stent System
- Applicant
- Medtronic Vascular
- PMA number
- P160043
- Supplement
- S010
- Product code
- NIQ
- Decision date
- 2017-11-07
- Classification
- Coronary Drug-eluting Stent
- Generic name
- Coronary drug-eluting stent
- Approval order statement
- Create a product group for the purpose of bacterial endotoxin testing using Limulus Amebocyte Lysate.
Current openFDA PMA Record#
- Device
- Resolute Onyx Zotarolimus-Eluting Coronary Stent System
- Applicant
- Medtronic Vascular
- PMA number
- P160043
- Supplement
- S010
- Product code
- NIQ
- Generic name
- Coronary drug-eluting stent
- Decision date
- 2017-11-07
- Decision code
- OK30
- Date received
- 2017-10-12
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Create a product group for the purpose of bacterial endotoxin testing using Limulus Amebocyte Lysate.