FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Dermal, For Aesthetic Use

PMA: P090016 · Supplement: S019 · Decision Mar 29, 2017
Classifications
1
FEI Numbers
29
Registration Numbers
29

Basic Information

Device Name
Implant, Dermal, For Aesthetic Use
Trade Name
BELOTERO BALANCE
PMA Number
P090016
Supplement Number
S019
Device Class
FDA Class 3
Product Code
LMH
Generic Name
Implant, dermal, for aesthetic use
Medical Specialty
Unknown
Advisory Committee
General, Plastic Surgery
Decision
Approved
Decision Code
APPR
Decision Date
March 29, 2017
Date Received
December 1, 2015
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval of the addition of temperature monitoring devices to trans-Atlantic shipments and changes to the incoming inspection procedure.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LMH Implant, Dermal, For Aesthetic Use