AFX ENDOVASCULAR AAA SYSTEM
FDA premarket approval P040002/S051 · decided 2014-07-11
Approval details
- PMA number
- P040002
- Supplement
- S051
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- AFX ENDOVASCULAR AAA SYSTEM
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Endologix, LLC
- Date received
- 2014-06-12
- Decision date
- 2014-07-11
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Irvine, CA
- Statement
- ALTERNATE POLYTETRAFLUOROETHYLENE (PTFE) RESIN.
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