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AART GLUTEAL IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K021839
510(k) Type
Traditional
Applicant
Aesthetic and Reconstructive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2002
Days to Decision
42 days
Submission Type
Summary

AART GLUTEAL IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K021839
510(k) Type
Traditional
Applicant
Aesthetic and Reconstructive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2002
Days to Decision
42 days
Submission Type
Summary