Exogenesis Hernia Mesh
K-Number: K191545 · 2019-09-26
ApplicantExogenesis Corporation
Decision Date2019-09-26
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Exogenesis Hernia Mesh is a medical device manufactured by Exogenesis Corporation. It received FDA 510(k) clearance on 2019-09-26 under approval number K191545. 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 Exogenesis Hernia Mesh?
Exogenesis Hernia Mesh is a medical device that received FDA 510(k) clearance on 2019-09-26. It is manufactured by Exogenesis Corporation. The 510(k) number is K191545.
When was Exogenesis Hernia Mesh approved by the FDA?
Exogenesis Hernia Mesh received FDA 510(k) clearance on 2019-09-26, under approval number K191545.
What company makes Exogenesis Hernia Mesh?
Exogenesis Hernia Mesh is manufactured by Exogenesis Corporation.
What is the FDA product code for Exogenesis Hernia Mesh?
The FDA product code for Exogenesis 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.