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Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal System

NCT01220505 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 66

Last updated 2019-12-19

No results posted yet for this study

Summary

The purpose of this Post Market Surveillance Validation is to document the performance and clinical outcomes of the Polaris Deformity Spinal System \& Trivium 3D Spinal Deformity Correction System.

Conditions

  • Spinal Deformity

Interventions

PROCEDURE

Surgery

All subjects will have spinal surgery between the levels of T1 and Ilium using the Polaris Deformity Spinal System

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Tammy Stinson · Zimmer Biomet

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2014-01-31
Completion
2014-01-31

Countries

  • United States
  • Puerto Rico

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 NCT01220505 on ClinicalTrials.gov