PMA P030047S029
- Device
- PRECISE, PRECISE RX AND PRECISE PRO RX NITINOL STENT SYSTEM
- Applicant
- Cordis US Corporation
- PMA number
- P030047
- Supplement
- S029
- Product code
- NIM
- Decision date
- 2015-11-25
- Classification
- Stent, Carotid
- Generic name
- Stent, carotid
- Approval order statement
- APPROVAL FOR REMOVAL OF PERFLUORO-OCTANOIC ACID (PFOA) FROM THE POLYTETRAFLUORO-ETHYLENE (PTFE) TUBING.
Current openFDA PMA Record#
- Device
- PRECISE, PRECISE RX AND PRECISE PRO RX NITINOL STENT SYSTEM
- Applicant
- Cordis US Corporation
- PMA number
- P030047
- Supplement
- S029
- Product code
- NIM
- Generic name
- Stent, carotid
- Decision date
- 2015-11-25
- Decision code
- APPR
- Date received
- 2015-03-19
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR REMOVAL OF PERFLUORO-OCTANOIC ACID (PFOA) FROM THE POLYTETRAFLUORO-ETHYLENE (PTFE) TUBING.