Last synced on 20 December 2024 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
K230227
510(k) Type
Special
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2023
Days to Decision
27 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
K230227
510(k) Type
Special
Applicant
Deep Blue Medical Advances, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2023
Days to Decision
27 days
Submission Type
Summary