PMA P010041S007
- Device
- CARPENTIER-EDWARDS SUPRAANNULAR (S.A.V.) BIOPROSTHESIS, MODEL 2650
- Applicant
- Edwards Lifesciences, LLC
- Product code
- DYE
- Decision date
- 2005-04-08
- Generic name
- replacement Heart-valve
- Approval order statement
- CHANGE TO THE SUPPLIER OF POLYTETRAFLUOROETHYLENE (PTFE) YARN AND THREAD.
Current openFDA PMA Record
- Device
- CARPENTIER-EDWARDS SUPRAANNULAR (S.A.V.) BIOPROSTHESIS, MODEL 2650
- Applicant
- Edwards Lifesciences, LLC
- PMA number
- P010041
- Supplement
- S007
- Product code
- DYE
- Generic name
- replacement Heart-valve
- Decision date
- 2005-04-08
- Decision code
- OK30
- Date received
- 2005-03-21
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE TO THE SUPPLIER OF POLYTETRAFLUOROETHYLENE (PTFE) YARN AND THREAD.