Evaluation of the Fortilink IBF System With TETRAfuse Technology

Completed

Conditions studied: Cervical and Lumbar Fusion

In brief

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

Key facts

Study ID

NCT03699891

Run by

RTI Surgical

People needed

119

Starts

2018-11-06

Expected to finish

2019-01-15

Last updated by the study team

2019-10-02

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient must have had an attempted implant of the Fortilink IBF System

You may not qualify if…

• There are no exclusion criteria

Where it is running

• Los Angeles Orthopedic Institute — Sherman Oaks, California, United States
• Rocky Mountain Spine — Lone Tree, Colorado, United States
• Florida Back Institute — Boca Raton, Florida, United States
• Spine Institute of South Florida — Delray Beach, Florida, United States
• OrthoBethesda — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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