Trials / Active Not Recruiting
Active Not RecruitingNCT05762588
JuggerKnot With Broadband PMCF Study
JuggerKnot With BroadBand Tape Post Market Clinical Follow-Up Study
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (estimated)
- Sponsor
- Riverpoint Medical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to collect post-market clinical follow-up data, which is needed to confirm the safety and performance of the JuggerKnot device and meet existing EU regulatory requirements.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Juggerknot with Broadband tape | The JuggerKnot system is comprised of a coreless sleeve structure and suture. The anchors are intended for use in soft tissue to bone fixation by bunching against the bone when deployed. The anchor sleeve material is polyester. Suture materials are ultra-high molecular weight polyethylene. The device has 510K FDA clearance. |
Timeline
- Start date
- 2023-11-30
- Primary completion
- 2025-09-30
- Completion
- 2025-12-30
- First posted
- 2023-03-09
- Last updated
- 2025-08-17
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05762588. Inclusion in this directory is not an endorsement.