PMA P050006S003
- Device
- GORE HELEX SEPTAL OCCLUDER
- Applicant
- W. L. Gore & Associates, Inc.
- PMA number
- P050006
- Supplement
- S003
- Product code
- MLV
- Decision date
- 2007-05-18
- Classification
- Transcatheter Septal Occluder
- Generic name
- Transcatheter septal occluder
- Approval order statement
- MODIFICATION OF THE DESTRUCTIVE TESTING PROCEDURE FOR THE NITINOL WIRE USED IN THE MANUFACTURE OF THE DEVICE.
Current openFDA PMA Record#
- Device
- GORE HELEX SEPTAL OCCLUDER
- Applicant
- W. L. Gore & Associates, Inc.
- PMA number
- P050006
- Supplement
- S003
- Product code
- MLV
- Generic name
- Transcatheter septal occluder
- Decision date
- 2007-05-18
- Decision code
- OK30
- Date received
- 2007-04-19
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- MODIFICATION OF THE DESTRUCTIVE TESTING PROCEDURE FOR THE NITINOL WIRE USED IN THE MANUFACTURE OF THE DEVICE.