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

RTI Surgical60 enrolled

Overview

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

This is a multi-center, post-market, retrospective study design to collect safety and performance data for patients implanted with the Streamline OCT System. The study will include a minimum of 58 patients at a minimum of 3 sites in the United States. The study will enroll at a minimum of 5 subjects implanted with the occipital plate.

Study Type

OBSERVATIONAL

Enrollment

Conditions

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

Interventions

Streamline Occipito-Cervico-Thoracic Spinal Fixation SystemDEVICE

Spinal Fixation

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Subject must have had an implant of the OCT System. Exclusion Criteria: * No exclusion criteria.

Locations (2)

Las Vegas Neurosurgical Institute

Las Vegas, Nevada, United States

Spine Nevada

Reno, Nevada, United States

Outcomes

Primary Outcomes

Evaluate time to demonstration of fusion.

Time frame: 12 months

Data from ClinicalTrials.gov

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