Elbow Outcomes Clinical Study (WELBOW)

Inclusion Criteria

• •18 years or older at the time of the informed consent or the non-opposition (when applicable).
• •Informed and willing to sign an informed consent form approved by IRB or EC (when applicable).
• •Willing and able to comply with the requirements of the study protocol.
• •For prospective inclusion: Considered for treatment with one Wright Medical Elbow arthroplasty or fracture devices included in this study (primary or revision).
• •For ambispective inclusion
• •1. Must have undergone an Elbow arthroplasty or fracture with one Wright Medical Elbow studied device between the date of the first Site Initiation Visit (SIV) and until 4.5 years prior this one in order to have at least the 5 years follow-up visit prospectively. Ambispective patients who were explanted prior the date of the first SIV will be included.
• •2. Must have complete Information available for each completed visit (demographics, preoperative information, surgery information, device details)\*.