ANEURX STENT GRAFT SYSTEM
FDA premarket approval P990020/S001 · decided 1999-12-10
Approval details
- PMA number
- P990020
- Supplement
- S001
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ANEURX STENT GRAFT SYSTEM
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Medtronic Vascular
- Date received
- 1999-11-18
- Decision date
- 1999-12-10
- Days to decision
- 22 days
- Decision code
- OK30
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Rosa, CA
- Statement
- The 30-Day Notice requested a change to add a supplier of expanded stents.
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