Atlas FDA

JUVÉDERM® VOLUMA ® XC

FDA premarket approval P110033/S079 · decided 2024-05-02

Approval details

PMA number
P110033
Supplement
S079
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
JUVÉDERM® VOLUMA ® XC
Generic name
Implant, dermal, for aesthetic use
Applicant
Allergan
Date received
2023-11-06
Decision date
2024-05-02
Days to decision
178 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Irvine, CA
Statement
Approval for the proposed device-specific use training program for P110033/S070 JUVEDERM® VOLUMA ® XC to improve temple hollowing

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510(k) clearances by this applicant

RecordFirmDate
NATRELLE INSPIRA Single Use Sizers for Gel Implants (K203229)Allergan2021-06-02
TrueTear Intranasal Tear Neurostimulator (K193589)Allergan2020-08-31
Natrelle 133 Plus MICROCELL Tissue Expander (K180826)Allergan2018-12-21
Natrelle 133S Tissue Expander (K182054)Allergan2018-08-29
TrueTear Intranasal Tear Neurostimulator (DEN170086)Allergan2018-05-17
SERI SURGICAL SCAFFOLD (K123128)Allergan2013-04-25