S&P of Q-Fix™ All-Suture Anchor System



Status:Recruiting
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:3/21/2019
Start Date:September 8, 2018
End Date:December 8, 2020
Contact:Kirsten Wall, MHS
Email:kirsten.wall@smith-nephew.com
Phone:1-720-338-9460

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Safety and Performance of Q-Fix™ All-Suture Anchor System

Post-market clinical follow-up needed to address existing clinical data and gaps on the
existing Q-Fix™ device and meet existing MDD/MEDDEV requirements


Inclusion Criteria:

- Subject has undergone arthroscopic instability repair with QFix™ All-Suture Anchor
System

- Subject was ≥ 18 of age at time of surgery

Exclusion Criteria:

- Subject is ≤ 6 months post-operative

- Subject is entered in another investigational drug, biologic, or device study or has
been treated with an investigational product within 12 months post-operative.
We found this trial at
4
sites
Columbia, South Carolina 29203
Principal Investigator: Guillaume Dumont, MD
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Columbia, SC
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Chicago, Illinois 60201
Principal Investigator: Jason Koh, MD, MBA
Phone: 847-503-4295
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Chicago, IL
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New Orleans, Louisiana 70112
Principal Investigator: Mary Mulcahey, MD
Phone: 504-988-0653
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from
New Orleans, LA
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Washington, District of Columbia 20037
Principal Investigator: Scott C. Faucett, MD
Phone: 202-912-8480
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from
Washington,
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