Atlas FDA

GEL-ONE

FDA premarket approval P080020/S021 · decided 2016-07-25

Approval details

PMA number
P080020
Supplement
S021
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GEL-ONE
Generic name
Acid, hyaluronic, intraarticular
Applicant
Seikagaku Corp.
Date received
2016-06-30
Decision date
2016-07-25
Days to decision
25 days
Decision code
OK30
Product code
MOZ
Advisory committee
Orthopedic
Expedited review
No
Location
Tokyo
Statement
Update the application software for the existing intrinsic viscosity measuring system used for the manufacture of Gel-One.

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510(k) clearances by this applicant

RecordFirmDate
HADGEL, 4 GRAM/SYRINGE (K011544)Seikagaku Corp.2001-08-15