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 |
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
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
Chicago, Illinois 60201
Principal Investigator: Jason Koh, MD, MBA
Phone: 847-503-4295
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Columbia, South Carolina 29203
Principal Investigator: Guillaume Dumont, MD
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New Orleans, Louisiana 70112
Principal Investigator: Mary Mulcahey, MD
Phone: 504-988-0653
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Washington, District of Columbia 20037
Principal Investigator: Scott C. Faucett, MD
Phone: 202-912-8480
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