PMA P990017S001
- Device
- ANCURE TUBE AND BIFURCATED SYSTEMS & ILIAC BALLOON CATHETER
- Applicant
- Boston Scientific Corp
- PMA number
- P990017
- Supplement
- S001
- Product code
- MIH
- Decision date
- 1999-10-20
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Approval order statement
- Approval for a new manufacturing facility located at Guidant Corporation, 1525 O'Brien Drive, Menlo Park, CA.
Current openFDA PMA Record
- Device
- ANCURE TUBE AND BIFURCATED SYSTEMS & ILIAC BALLOON CATHETER
- Applicant
- Boston Scientific Corp
- PMA number
- P990017
- Supplement
- S001
- Product code
- MIH
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Decision date
- 1999-10-20
- Decision code
- APPR
- Date received
- 1999-09-30
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Express GMP Supplement
- Approval order statement
- Approval for a new manufacturing facility located at Guidant Corporation, 1525 O'Brien Drive, Menlo Park, CA.