BONESUPPORT: CERAMENT wins full FDA approval in Spine Fusion procedures
Yesterday after the market close, BONESUPPORT announced that CERAMENT BONE VOID FILLER, the company's core synthetic bone graft technology, has been granted FDA approval on the Spine Interbody Fusion procedure, following the 510 (k) submission in Q1 2024. We are certainly surprised about the quickBonesupport Holding AB is a Sweden-based orthobiologics company. It develops and commercialize injectable bioceramic bone graft substitutes which remodel to host bone and have the capability to elute drugs directly into the bone void. The marketed synthetic bone graft substitutes are CERAMENT BVF, CERAMENT G and CERAMENT V, which are based on the CERAMENT technology platform. The products are commercially available in Europe and the United States, as well as in India, Malaysia, Oman and Singapore. The products are developed to treat patients with fractures and bone voids caused by trauma and related surgery, as well as caused by infection or diseases, such as chronic osteomyelitis, revision arthroplasty and infected diabetic foot.
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