Post-Marketing Clinical Follow-Up of a Spine Implant

Trial ID or NCT#

NCT03180749

Status

not recruiting iconNOT RECRUITING

Purpose

Post-Marketing Clinical Follow-up of an Anular Closure System (Barricaid®) to Confirm Comparability of Outcome between Devices with Subcomponents from Two Different Suppliers

Official Title

Post-Marketing Clinical Follow-up of an Anular Closure System (Barricaid®) to Confirm Comparability of Outcome Between Devices With Subcomponents From Two Different Suppliers

Eligibility Criteria

Ages Eligible for Study: Older than 18
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: Yes
Inclusion Criteria:
  1. * Each site will enroll all patients who were implanted with a Barricaid with an anchor manufactured by the second manufacturer.* Patients must be 18 years of age or older and able to understand and consent to participate in the study.
Exclusion Criteria:
  1. * Not defined

Investigator(s)

John Kleimeyer, MD
John Kleimeyer, MD
Spine surgeon, Orthopaedic surgeon, Orthopaedic surgeon
Clinical Assistant Professor, Orthopaedic Surgery