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Streamline Occipito-Cervico-Thoracic System Post-Market Clinical Follow-up

NCT04171544 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2020-10-27

No results posted yet for this study

Summary

This is a multi-center, post-market, retrospective study design to collect safety and performance data for patients implanted with the Streamline OCT System.

Conditions

  • Spinal Stenosis Occipito-Atlanto-Axial
  • Spinal Disease
  • Spinal Stenosis Cervical
  • Spinal Stenosis Cervicothoracic Region
  • Spinal Instability

Interventions

DEVICE

Streamline Occipito-Cervico-Thoracic Spinal Fixation System

Spinal Fixation

Sponsors & Collaborators

  • RTI Surgical

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-06
Primary Completion
2020-03-31
Completion
2020-03-31
FDA Device
Yes

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 NCT04171544 on ClinicalTrials.gov