FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Dermal, For Aesthetic Use

PMA: P090016 · Supplement: S003 · Decision Dec 7, 2012
Classifications
1
FEI Numbers
29
Registration Numbers
29

Basic Information

Device Name
Implant, Dermal, For Aesthetic Use
Trade Name
BELOTERO BALANCE DERMAL FILTER
PMA Number
P090016
Supplement Number
S003
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
December 7, 2012
Date Received
October 10, 2012
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.

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