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BioFiber Scaffold Post-Market Observational Study

Full Thickness Rotator Cuff Tear Clinical Trial

Official title:
BioFiber and BioFiber-CM Absorbable Biologic Scaffold for Soft Tissue Repair and Reinforcement Post-Market Surveillance Clinical Study

Clinical Trial Summary

The aim of this study is to collect and report data from a consecutive series of patients implanted with these products as part of a post-market surveillance plan for CE Mark approval in the European Union.

Clinical Trial Description

Rhe BioFiberTM Scaffold post-market surveillance study is a prospective, single arm, multi-center observational study with sites in the US and France. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01849458
Study type Observational
Source Tornier, Inc.
Contact
Status Completed
Phase N/A
Start date March 2013
Completion date April 2015
View Details
See also
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