Zimmer Biomet Spine
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Regulatory
FDA approves first of its kind device to treat pediatric patients with progressive idiopathic scoliosis
SILVER SPRING, Md., Aug. 16, 2019 /PRNewswire/ — The U.S. Food and Drug Administration today approved the first spinal tether device intended to…
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Spine
Zimmer Biomet Spine Announces Mobi-C® Cervical Disc Seven-Year Follow-Up Data Published in International Journal of Spine Surgery
WARSAW, Ind., March 28, 2018 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today announced…
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