This long-term outcomes study is designed to collect safety and efficacy data on designated, commercially available, hip arthroplasty products.
Man or woman >18 years
Subjects with indication of arthroplasty surgery with Corin hip devices which are under assessment as part of this PMCF study
Subjects who agreed for study participation.
Subjects with existing tumour and/or particularly high surgical risk-
Subjects with anaesthetic risk class IV or higher
Subjects under guardianship and/or unable to follow procedures or matters related to the study (examples: Illiterate, recent psychotic or mania disorders and / or inability to comply with usual follow-up visits.)
Contraindications for arthroplasty with a Corin hip devices as per product IFU
Corin
Lead sponsor