K232924
- 510(k) number
- K232924
- Device name
- T-Line® Hernia Mesh
- Applicant
- Deep Blue Medical Advances, Inc. NC · US
- Product code
- FTL — Mesh, Surgical, Polymeric
- Decision date
- 2023-10-18
- Date received
- 2023-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K232924.pdf
Official FDA record: K232924
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.