Trials / Completed
CompletedNCT03782298
Safety and Performance of PEEK Anchors in Extremities
Safety and Performance of PEEK Anchors (DYNOMITE, SPYROMITE, RAPTOMITE, FOOTPRINT Ultra PK SL) in Extremities
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 140 (actual)
- Sponsor
- Smith & Nephew, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Safety and performance of the study devices in extremities up to 12 months post-surgery
Conditions
- Medial or Lateral Instability Repairs/Reconstructions
- Hallux Valgus Repairs
- Achilles Tendon Repairs/Reconstructions
- Midfoot Reconstructions
- Metatarsal Ligament/Tendon Repairs/Reconstructions
- Bunionectomy
- Scapholunate Ligament Reconstructions
- Ulnar
- Lateral Epicondylitis Repair
- Bicep Tendon Reattachments
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Spyromite, Dynomite, Raptomite, Footprint Ultra PK SL | PEEK Suture Anchors, which include: * SPYROMITE™ 2.0 PK Suture Anchor with Needles * DYNOMITE™ 2.0 PK Suture Anchor with Needles * RAPTORMITE™ 3.0 Suture Anchor with Needles * FOOTPRINT™ Ultra PK SL Suture Anchor |
Timeline
- Start date
- 2019-03-12
- Primary completion
- 2019-10-10
- Completion
- 2019-10-10
- First posted
- 2018-12-20
- Last updated
- 2024-10-01
- Results posted
- 2024-09-24
Locations
4 sites across 2 countries: United States, Canada
Source: ClinicalTrials.gov record NCT03782298. Inclusion in this directory is not an endorsement.