UROLUME ENDOPROSTHESIS
FDA premarket approval P920023/S018 · decided 2004-10-15
Approval details
- PMA number
- P920023
- Supplement
- S018
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- UROLUME ENDOPROSTHESIS
- Generic name
- STENT, URETHRAL, BULBOUS, PERMANENT OR SEMI-PERMANENT
- Applicant
- Boston Scientific Corp
- Date received
- 2004-09-30
- Decision date
- 2004-10-15
- Days to decision
- 15 days
- Decision code
- APPR
- Product code
- MES
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Marlboro, MA
- Statement
- APPROVAL FOR THE USE OF NUSIL MED 360 (1,000 CP) TO LUBRICATE THE DELIVERY TOOL AND TO CHANGE THE POSITIONING OF THE GRAPPLE PORTION OF THE DELIVERY TOOL.
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