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Prosidyan™ Announces FDA 510(k) Clearance of FIBERGRAFT™BG Putty – Bone Graft Substitute

Confidential

April 3, 2015

Warren, NJ, March 26, 2015 –(PR.com)– NJ-based Prosidyan™ (www.prosidyan.com), developer of proprietary fiber-based bioactive glass products, announced today that it has received FDA 510(k) clearance of FIBERGRAFT™ BG Putty – Bone Graft Substitute. This is the second generation product in

Stryker Spine Receives FDA Clearance for New Lumbar Plating System

Confidential

April 2, 2015

ALLENDALE, N.J., March 25, 2015 /PRNewswire/ — Stryker Corporation’s Spine Division announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the LITe® Plate System, an Anterior and Lateral Lumbar Plate System.  The LITe Plate

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