Monster Screw System Post-Market Clinical Follow-Up Study
NCT05190159 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82
Last updated 2022-09-23
Summary
Post-market clinical follow-up study on the Monster Screw System
Conditions
- Ankle Injuries
- Foot Injury
Interventions
- DEVICE
-
Monster Screw System
Subjects who have undergone a foot and/or ankle procedure involving the index device
Sponsors & Collaborators
-
Paragon 28
lead INDUSTRY
Principal Investigators
-
Jacy Legue · Paragon 28
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-01-26
- Primary Completion
- 2022-09-14
- Completion
- 2022-09-21
- FDA Device
- Yes
Countries
- United States
Study Locations
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