T-Line® Hernia Mesh
K-Number: K232924 · 2023-10-18
ApplicantDeep Blue Medical Advances, Inc.
Decision Date2023-10-18
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
T-Line® Hernia Mesh is a medical device manufactured by Deep Blue Medical Advances, Inc.. It received FDA 510(k) clearance on 2023-10-18 under approval number K232924. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the T-Line® Hernia Mesh?
T-Line® Hernia Mesh is a medical device that received FDA 510(k) clearance on 2023-10-18. It is manufactured by Deep Blue Medical Advances, Inc.. The 510(k) number is K232924.
When was T-Line® Hernia Mesh approved by the FDA?
T-Line® Hernia Mesh received FDA 510(k) clearance on 2023-10-18, under approval number K232924.
What company makes T-Line® Hernia Mesh?
T-Line® Hernia Mesh is manufactured by Deep Blue Medical Advances, Inc..
What is the FDA product code for T-Line® Hernia Mesh?
The FDA product code for T-Line® Hernia Mesh is FTL.
Other Devices by Deep Blue Medical Advances, Inc.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.