Safety and Performance of PEEK Anchors (Dynomite, Spyromite, Raptomite) in Extremities
| Status: | Not yet recruiting |
|---|---|
| Conditions: | Orthopedic, Orthopedic |
| Therapuetic Areas: | Orthopedics / Podiatry |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/28/2019 |
| Start Date: | March 31, 2019 |
| End Date: | February 28, 2021 |
| Contact: | Sandra Navarrete |
| Email: | Sandra.Navarrete@smith-nephew.com |
| Phone: | 512-895-1086 |
Safety and Performance of PEEK Anchors (Dynomite, Spyromite, Raptormite, Footprint Ultra PK SL) in Extremities
Safety and performance of the study devices in extremities over a time period of 6 months
after intervention.
after intervention.
Inclusion Criteria:
- Subjects who have undergone extremity joint repair using the study devices.
- Subjects aged 18 years and older at the time of surgery.
Exclusion Criteria:
- Subject is entered in another investigational drug, biologic, or device study or has
been treated with an investigational product within 12 months post-operative.
- Subjects who are < 3 months post-operative
We found this trial at
2
sites
Charlotte, North Carolina 28207
Principal Investigator: Carroll Jones, MD
Phone: 704-323-3697
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Chardon, Ohio 44024
Principal Investigator: Mark Mendeszoon, DPM
Phone: 414-630-2388
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