Atlas FDA

SOLESTA INJECTABLE GEL

FDA premarket approval P100014/S017 · decided 2015-01-21

Approval details

PMA number
P100014
Supplement
S017
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
SOLESTA INJECTABLE GEL
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Palette Life Sciences
Date received
2014-11-19
Decision date
2015-01-21
Days to decision
63 days
Decision code
APPR
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Santa Barbara, CA
Statement
APPROVAL FOR PATIENT LABELING CHANGES.

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