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MDR EZ Pass and Precision Flexible Reamer

NCT03914703 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 73

Last updated 2025-07-01

Study results available
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Summary

The objective of this study is to confirm the safety and performance on the EZPass Suture Passer Instrumentation and the Precision Flexible Reamer Instrumentation.

Conditions

  • Anterior Cruciate Ligament Injury
  • Rotator Cuff Tear

Interventions

PROCEDURE

EZ Pass Suture Passer

Instruments used to help with rotator cuff or ACL repair

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Erin Osborn · Zimmer Biomet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-08
Primary Completion
2023-12-31
Completion
2024-04-08

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03914703 on ClinicalTrials.gov