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Clinical Trial Summary

The purpose of this study is to collect data needed to satisfy the European Union (EU) Medical Device Regulation (MDR) clinical post-market surveillance (PMS) and reporting requirements, and to support future regulatory submissions and peer-reviewed publications on device performance and safety.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05067543
Study type Observational
Source Tornier, Inc.
Status Enrolling by invitation
Start date September 12, 2021
Completion date December 1, 2033

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