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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
DeviceCOSMODERM 1 HUMAN-BASED COLLAGEN, COSMODERM 2 HUMAN-BASED COLLAGEN AND COSMOPLAST HUMAN-BASED COLLAGEN
Classification Nameimplant, dermal, for aesthetic use
Generic Nameimplant, dermal, for aesthetic use
Applicant
Allergan
71 south los carneros road
goleta, CA 93117-5506
PMA NumberP800022
Supplement NumberS050
Date Received05/16/2001
Decision Date03/11/2003
Product Code
LMH[ Registered Establishments with LMH ]
Docket Number 03M-0114
Notice Date 03/28/2003
Advisory Committee General & Plastic Surgery
Supplement Typepanel track
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for cosmoderm 1 human-based collagen, cosmoderm 2 human-based collagen and cosmoplast human-based collagen. The indications for use are as follows: cosmoderm 1 human-based collagen and cosmoderm 2 human-based collagen are injected into the superficial papillary dermis for correction of soft tissue contour deficiencies, such as wrinkles and acne scars, and cosmoplast human-based collagen is injected into the mid to deep dermis for correction of soft tissue contour deficiencies, such as wrinkles and acne scars.
Approval Order Approval Order
Summary Summary of Safety and Effectiveness
Labeling Labeling
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