Miromatrix Biological Mesh for Hiatal Hernia Repair

Status Completed

Clinical Trial Summary

Miromatrix Medical has developed MIROMESH® - a new, noncrosslinked, acellular mesh derived from the highly vascularized porcine liver. MIROMESH received FDA 510(k) clearance with an indication for reinforcement of soft tissue on March 31, 2014 under K134033. 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 hiatal hernia repair.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02436681
Study type	Interventional
Source	Miromatrix Medical Inc.
Contact
Status	Completed
Phase	N/A
Start date	August 2015
Completion date	July 2018

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See also
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