Atlas FDA

DEFLUX INJECTABLE GEL

FDA premarket approval P000029/S027 · decided 2007-07-10

Approval details

PMA number
P000029
Supplement
S027
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
DEFLUX INJECTABLE GEL
Generic name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Applicant
Palette Life Sciences
Date received
2007-06-11
Decision date
2007-07-10
Days to decision
29 days
Decision code
OK30
Product code
LNM
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Santa Barbara, CA
Statement
CHANGE IN SHELF LIFE FOR A FILTER USED IN THE MANUFACTURING PROCESS OF THE DEVICE.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

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