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T-Line Hernia Mesh

Page Type
Cleared 510(K)
510(k) Number
K221556
510(k) Type
Traditional
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
181 days
Submission Type
Summary

T-Line Hernia Mesh

Page Type
Cleared 510(K)
510(k) Number
K221556
510(k) Type
Traditional
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
181 days
Submission Type
Summary