Streamline Occipito-Cervico-Thoracic System Post-Market Clinical Follow-up (OCT PMCF)

RTI Surgical

Status: Completed

Conditions: Spinal Disease; Spinal Instability; Spinal Stenosis Occipito-Atlanto-Axial; Spinal Stenosis Cervicothoracic Region; Spinal Stenosis Cervical

Treatments: Device: Streamline Occipito-Cervico-Thoracic Spinal Fixation System

Study type: Observational

Funder types: Industry

Identifiers

NCT04171544

1108-CL

Details and patient eligibility

About

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

Full description

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.

Enrollment: 60 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subject must have had an implant of the OCT System.

Exclusion criteria

• No exclusion criteria.