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Clinical Trial Summary

This study is a retrieval of database information regarding survivorship of the Comprehensive Shoulder System family of products. The primary objective of the retrieval is to collect data that will contribute to the post market surveillance requirements for this product and will provide feedback to design engineers, support marketing efforts and publications, and answer potential questions form reimbursement agencies.


Clinical Trial Description

The Comprehensive Shoulder System has been cleared by the FDA via premarket notifications. No experimental or investigational surgical techniques or devices will be used in this study. All devices and products will be used in accordance with their instructions for use and/or approved labeling. The aim of the Comprehensive Shoulder System is to improve shoulder function and reduce pain. One site will be used for this database retrieval. The number of patients involved will depend upon the size of the Comprehensive database available at Acromion, LLC. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03409718
Study type Observational [Patient Registry]
Source Zimmer Biomet
Contact
Status Active, not recruiting
Phase
Start date February 24, 2011
Completion date December 2026

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