AORFIX AA FLEXIBLE STENT GRAFT SYSTEM
FDA premarket approval P110032/S003 · decided 2013-06-18
Approval details
- PMA number
- P110032
- Supplement
- S003
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- AORFIX AA FLEXIBLE STENT GRAFT SYSTEM
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Lombard Medical Limited
- Date received
- 2013-05-20
- Decision date
- 2013-06-18
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Didcot
- Statement
- MODIFIED STERILIZATION CYCLE.
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