510(k) K232924

Device
T-Line® Hernia Mesh
Applicant
Deep Blue Medical Advances, Inc.
510(k) number
K232924
Product code
FTL
Decision
Substantially Equivalent (SESE)
Decision date
2023-10-18
Date received
2023-09-19
Regulation
878.3300
Classification name
Mesh, Surgical, Polymeric
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
William Perry
Address
701 W Main St. Suite 410 Durham NC US 27701 27701

FDA Registration Numbers

Source Documents

510(k) summary PDF

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