Centinel Spine has received certification under the European Union (EU) Medical Device Regulation (MDR) for its prodisc C Vivo and prodisc C Nova cervical total disc replacement (TDR) systems. The ...
The prodisc® C Vivo and prodisc® C Nova Cervical Total Disc Replacement (TDR) devices are now certified and CE-marked in accordance with the EU Medical Device Regulation (MDR) – the highest European ...
Record full-year 2024 prodisc® Total Disc Replacement (TDR) revenue of over $95 million in sales, up 38% over prior year. Full-year 2024 prodisc TDR sales broke records in both U.S. and International ...
(HealthDay)—Local facet joint contact pressures are not significantly altered during sagittal bending after the implantation of a ProDisc-C device at the C5 to C6 level in cadaveric human cervical ...
WEST CHESTER, PA, January 6, 2026 (EZ Newswire) -- Centinel Spine®, the leading global medical device company focused exclusively on treating cervical and lumbar spinal disease with the most complete ...
NEW YORK, Dec. 22, 2017 /CNW/ -- Centinel Spine, LLC (CS) is pleased to announce the acquisition of the worldwide assets of the prodisc® Total Disc Replacement portfolio from DePuy Synthes Products, ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Early composite clinical success showed similar outcomes ...
ZURICH, April 15 (Reuters) - Swiss medical device maker Synthes said the reimbursement of its artificial spine disc ProDisc-C in the United States has disappointed so far. "Only one private insurer ...
(HealthDay News) – Local facet joint contact pressures are not significantly altered during sagittal bending after the implantation of a ProDisc-C device at the C5–C6 level in cadaveric human cervical ...
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