Atlas FDA

BELOTERO BALANCE DERMAL FILLER

FDA premarket approval P090016/S013 · decided 2016-05-24

Approval details

PMA number
P090016
Supplement
S013
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
BELOTERO BALANCE DERMAL FILLER
Generic name
Implant, dermal, for aesthetic use
Applicant
Merz North America, Inc.
Date received
2014-11-28
Decision date
2016-05-24
Days to decision
543 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Franksville, WI
Statement
Sharing equipment used during the manufacture of belotero balace dermal filler across other product lines.

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510(k) clearances by this applicant

RecordFirmDate
DESCRIBE PFD Patch (K172689)Merz North America, Inc.2017-11-29