Atlas FDA

Revanesse Versa+

FDA premarket approval P160042/S012 · decided 2020-10-13

Approval details

PMA number
P160042
Supplement
S012
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Revanesse Versa+
Generic name
Implant, dermal, for aesthetic use
Applicant
Prollenium Medical Technologies, Inc.
Date received
2020-07-15
Decision date
2020-10-13
Days to decision
90 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Aurora
Statement
Approval to change the shelf-life from 18 months to 24 months for Revanesse Versa+

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