KB Medical Receives CE Mark Approval for AQrate Spinal Robotic Assistance System
KB Medical received approval under the CE Mark for its AQrate™ Robotic Assistance system, indicated for use in general spinal surgery. Jun 14, 2016
Zimmer Biomet Acquires Compression Therapy Concepts
Zimmer Biomet acquired Compression Therapy Concepts, provider of devices to prevent deep venous thrombosis following a variety of surgical procedures. CTC will operate as a wholly-owned subsidiary of Zimmer Biomet. Transaction terms were not disclosed. Jun 13, 2016
ISTO Technologies Acquired by Private Equity Firm
The commercial operations of ISTO Technologies, an orthobiologics company, were acquired by private equity firm Thompson Street Capital Partners. Transaction terms were not disclosed. Jun 13, 2016
AlloSource Launches AlloFuse Cortical Fibers and Fiber Boats
AlloSource launched AlloFuse® Cortical Fibers and AlloFuse Fiber Boat demineralized cortical fiber allografts for a variety of spine and orthopaedic procedures. Jun 13, 2016
Spineart Announces BAGUERA C Milestone
As of 2Q15, >15,000 of Spineart’s BAGUERA® C cervical disc replacement devices have been successfully implanted worldwide. Jun 13, 2016
Amedica Submits Response to FDA for Clearance of Composite Interbody Spinal Device
Amedica submitted its responses to FDA in relation to the CASCADE clinical trial, and expects a final determination from FDA within 60 days. Jun 13, 2016
curasan to Expand in the U.S. and China
curasan will invest in targeted expansion of sales and marketing activities in the U.S. and China. The company markets CERASORB® bone void filler products. Jun 13, 2016
Titan Spine Enhances Endoskeleton Warranty
Titan Spine is amending its device warranty to provide a free replacement if any Endoskeleton® interbody fusion devices delaminate or generate particulate debris during implantation. Jun 13, 2016
SI-BONE Receives 510(k) Clearance on Updated Indication for iFuse Implant
SI-BONE received FDA 510(k) clearance of a modified indication for the iFuse Implant System®, noting that clinical studies have demonstrated its ability to improve pain, patient function and quality of life. Jun 13, 2016
Amplitude Surgical Files for ANATOMIC Knee 510(k)
Amplitude Surgical filed for FDA 510(k) clearance of its posterior stabilized ANATOMIC® knee prosthesis. Jun 09, 2016
