PMA P900043S018
- Device
- Crossflex Lc Balloon Expandable Stent With Otw Delivery Syst
- Applicant
- CORDIS CORP.
- PMA number
- P900043
- Supplement
- S018
- Decision date
- 2000-02-25
Current openFDA PMA Record
- Device
- CROSSFLEX LC BALLOON EXPANDABLE STENT WITH OTW DELIVERY SYSTEM
- Applicant
- Cordis Corp.
- PMA number
- P900043
- Supplement
- S018
- Product code
- MAF
- Generic name
- STENT, CORONARY
- Decision date
- 2000-02-25
- Decision code
- APPR
- Date received
- 1999-11-01
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Postapproval Study Protocol
- Approval order statement
- Approval of 5-year post approval study.