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Miromatrix Biological Mesh for Ventral Hernia Repair — MIROMESH PM-1  

Ventral Hernia Clinical Trial

Official title:
A Prospective Post-Market Clinical Evaluation of Miromatrix Biological Mesh for Ventral Hernia Repair

Clinical Trial Summary

This study is being conducted to gather long-term data of the performance of the Miromatrix Biological Mesh.

Clinical Trial Description

Miromatrix Medical Inc. has developed a new biologic mesh, called MIROMESH®. MIROMESH received FDA 510(k) clearance with an indication for reinforcement of soft tissue on March 31, 2014 under K134033. Miromatrix Biologic Mesh is a non cross-linked, acellular surgical mesh that is derived from the highly vascularized porcine liver. This study will serve to provide clinicians with high-quality clinical data in order to provide them with a higher degree of confidence when selecting MIROMESH for ventral hernia repair. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02408458
Study type Interventional
Source Miromatrix Medical Inc.
Contact
Status Withdrawn
Phase N/A
Start date June 2015
Completion date April 2016
View Details
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