Study design: monocentric, retrospective, observational and post-market clinical study. Purpose: To demonstrate the safety and performance of CoCrMo LOCK bipolar femoral heads. The eligible study population is represented by the entire population that underwent a hip replacement with CoCrMo LOCK bipolar femoral heads from 1st January 2023 onwards at the site in accordance with the indication for use of the product.
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Evaluation of the revision rate of CoCrMo LOCK Bipolar femoral heads at 24 months after surgery.
Timeframe: At 24 months after intraoperative visit