KB Medical Receives CE Mark Approval for AQrate Spinal Robotic Assistance System
KB Medical received approval under the CE Mark for its AQrateâ„¢ Robotic Assistance system, indicated for use in general spinal...
Jun 14, 2016,
KB Medical Receives CE Mark Approval for AQrate Spinal Robotic Assistance System
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...
Jun 13, 2016, Julie Vetalice
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...
Jun 13, 2016, Julie Vetalice
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, Julie Vetalice
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, Julie Vetalice
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, Julie Vetalice
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®...
Jun 13, 2016, Julie Vetalice
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...
Jun 13, 2016, Julie Vetalice
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...
Jun 13, 2016, Julie Vetalice
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, Julie Vetalice
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