Atlas FDA

DEFLUX INJECTABLE GEL

FDA premarket approval P000029/S080 · decided 2016-02-23

Approval details

PMA number
P000029
Supplement
S080
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
DEFLUX INJECTABLE GEL
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Palette Life Sciences
Date received
2015-03-03
Decision date
2016-02-23
Days to decision
357 days
Decision code
APPR
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Santa Barbara, CA
Statement
Approval for modifications to Deflux labeling to reflect the findings of the post-approval study (PAS).

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510(k) clearances by this applicant

RecordFirmDate
Barrigel Injectable Gel (K220641)Palette Life Sciences2022-05-26