Last synced on 30 September 2022 at 11:05 pm

T-Line Hernia Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193144
510(k) Type
Traditional
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2020
Days to Decision
138 days
Submission Type
Summary

T-Line Hernia Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193144
510(k) Type
Traditional
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2020
Days to Decision
138 days
Submission Type
Summary