TB-MED – BIOCERAMED
Prospective Multicenter Observational Study on the use of NEOCEMENT ® for the Treatment of Bone DefectsRegistry-based studyThis study is a post-market, multicenter, prospective, single arm observational registry that aims to collect performance and safety clinical data of NEOCEMENT (CE marked device) in the treatment of bone defects as part of routine clinical practice. The results of the Clinical Investigation shall be used as clinical evidence for clinical evaluation of the device aiming for submission to the new Medical Device Regulation (EU) 2017/745. This protocol does not include any new intended uses, new populations, new materials or design changes.
Population: adult | Intervention type: non-interventional medical device