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ARTIA Reconstructive Tissue Matrix Perforated

Page Type
Cleared 510(K)
510(k) Number
K162752
510(k) Type
Traditional
Applicant
LIFECELL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2017
Days to Decision
147 days
Submission Type
Summary

ARTIA Reconstructive Tissue Matrix Perforated

Page Type
Cleared 510(K)
510(k) Number
K162752
510(k) Type
Traditional
Applicant
LIFECELL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2017
Days to Decision
147 days
Submission Type
Summary