Zimmer Biomet Shoulder Arthroplasty PMCF
NCT04984291
This study is recruiting at 2 US sites in 2 states, according to its ClinicalTrials.gov record last updated .
Summary
The objectives of this study are to confirm the safety, performance, and clinical benefits of Zimmer Biomet Shoulder Arthroplasty Systems and its instrumentation in primary or revision shoulder arthroplasty. These objectives will be assessed using standard scoring systems, radiographic evidence, and adverse event records. Safety of the system will be assessed by monitoring the frequency an incidence of adverse events.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Shoulder Fractures
- Shoulder Arthritis
- Shoulder Osteoarthritis
- Shoulder Deformity
- Shoulder Injuries
- Shoulder Pain
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 20 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Zimmer Biomet
- Last updated on ClinicalTrials.gov
- April 28, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Colorado · 1
- Panorama Orthopaedic and Spine Center · Golden, CO
Utah · 1
- Intermountain Health · Murray, UT
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.