POWERLINK SYSTEM WITH VISIFLEX DELIVERY CATHETER
FDA premarket approval P040002/S008 · decided 2007-01-18
Approval details
- PMA number
- P040002
- Supplement
- S008
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- POWERLINK SYSTEM WITH VISIFLEX DELIVERY CATHETER
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Endologix, LLC
- Date received
- 2006-12-19
- Decision date
- 2007-01-18
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Irvine, CA
- Statement
- ADDING AN ADDITIONAL NON-DESTRUCTIVE LOAD TEST.
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