ANCURE ENDOGRAFT SYSTEM
FDA premarket approval P990017/S016 · decided 2001-08-17
Approval details
- PMA number
- P990017
- Supplement
- S016
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- ANCURE ENDOGRAFT SYSTEM
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Boston Scientific Corp
- Date received
- 2001-04-16
- Decision date
- 2001-08-17
- Days to decision
- 123 days
- Decision code
- APPR
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL FOR CHANGES TO DELIVERY CATHETER IPSILATERAL CAPSULE AND CONTRALATERAL PULLWIRE.
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