T-Line Hernia Mesh
K-Number: K193144 · 2020-03-30
ApplicantDeep Blue Medical Advances, Inc.
Decision Date2020-03-30
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 2020-03-30 under approval number K193144. 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 2020-03-30. It is manufactured by Deep Blue Medical Advances, Inc.. The 510(k) number is K193144.
When was T-Line Hernia Mesh approved by the FDA?
T-Line Hernia Mesh received FDA 510(k) clearance on 2020-03-30, under approval number K193144.
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.
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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.