Observational Study for the Evaluation of the Clinical Performance and Safety Profile of the GALAXY FIXATION™ System and Orthofix Implantable Devices: GALAXY Study

Inclusion Criteria: 1. The patient directly or indirectly (through a respondent) expressed his willingness to participate in the Study by signing and dating informed consent. 2. Patient who had a regular indication for the following surgical intervention with the GALAXY FIXATION™ System and Orthofix implantable devices according to manufacturer's IFUs: * fractures of the long bones or; * Vertically stable pelvic fractures or vertically unstable pelvic fractures as a treatment adjunct. 3. Patients equal or older than 29 days. 4. Patients who had a regular indication for external fixation according to the investigator criteria. 5. Patients with clinical data registered in her/his medical records sufficient to assess the safety and efficacy endpoints of the study Exclusion Criteria: 1. The patient is participating in other clinical studies or did he/she participate in the 3 months before signing the informed consent in other clinical studies. 2. The patient needed the application of or had already in-situ concomitant devices that couldn't be safely removed (except for permitted concomitant devices). 3. The patient was treated with more than one GALAXY FIXATION™ System or non Orthofix implantable devices. 4. Patient who had mental or physiological conditions who are unwilling or incapable of following postoperative care instructions. 5. Patient who had previous infections in the fracture area. 6. Patients who had malignancy in the fracture area. 7. Patients who had neuromuscular deficit or any other conditions that could influence the healing process. 8. Patients who had suspected or documented metal sensitivity reactions as it could result in a treatment failure in the intended population