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DURASPHERE INJECTABLE BULKING AGENT

FDA premarket approval P980053 · decided 1999-09-13

Approval details

PMA number
P980053
Trade name
DURASPHERE INJECTABLE BULKING AGENT
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Carbon Medical Technologies, Inc.
Date received
1998-12-31
Decision date
1999-09-13
Days to decision
256 days
Decision code
APPR
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
St. Paul, MN
Statement
This device is indicated for use in the treatment of adult women with stress urinary incontinence (SUI) due to intrinsic sphincter deficiency (ISD).

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