Atlas FDA

RADIESSE INJECTABLE IMPLANT

FDA premarket approval P050052/S034 · decided 2012-05-30

Approval details

PMA number
P050052
Supplement
S034
Supplement type
135 Review Track For 30-Day Notice
Trade name
RADIESSE INJECTABLE IMPLANT
Generic name
Implant, dermal, for aesthetic use
Applicant
Merz North America, Inc.
Date received
2011-12-22
Decision date
2012-05-30
Days to decision
160 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Franksville, WI
Statement
APPROVAL FOR A TEST RESULT EVALUATION PROCEDURE.

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510(k) clearances by this applicant

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