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FDA Premarket Approval Application Supplement approved for the Oxford Cementless Partial Knee – Zimmer Biomet

Written by | 6 Dec 2024

Zimmer Biomet Holdings, Inc. announced FDA Premarket Approval Application (PMA) Supplement approval for the Oxford Cementless Partial Knee. The approval is based on safety and effectiveness data from… read more.

510(k) FDA clearance of the VELYS Robotic-assisted solution for use in unicompartmental knee athroplasty procedures – DePuy Synthes

Written by | 8 Jul 2024

Johnson & Johnson MedTech announced that DePuy Synthes, The Orthopaedics Company of Johnson & Johnson, has received 510(k) FDA clearance for the clinical application of the VELYS™ Robotic-Assisted… read more.

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