Jun 11, 2020
MiRus(TM) Announces First Clinical Use of the MiRus(TM) 3DR(TM) Printed Lumbar Interbody Fusion System
Mar 03, 2020
Amplify(TM) Surgical Inc. Reaches Milestone of 300 Levels Treated with dualX® Expanding Interbody Fusion System
Oct 08, 2019
Amplify(TM) Surgical Inc. Announces 100th Level Treated with dualX(TM) Expanding Interbody Fusion System
Jun 04, 2019
Zavation Gains US FDA Clearance for the Ti3Z Interbody System (TLIF, T-PLIF, and PLIF)
May 14, 2019
ChoiceSpine(TM) Granted FDA Clearance for Two New Cervical Spinal Fusion Devices
Apr 02, 2019
Amplify(TM) Surgical, Inc. Exhibits Dual Expanding Technology at International Spine Conference
Mar 06, 2019
Amplify(TM) Surgical, Inc. Announces First Surgical Cases with dualX(TM) Dual Expanding Interbody Fusion System
Feb 13, 2019
Inspired Spine releases study on the Clinical and Radiological outcomes of Oblique Lateral Lumbar Interbody Fusion
Oct 31, 2018
Innovasive(TM) Granted FDA Clearance for DualX(TM) Expanding Interbody Spinal Device
Sep 26, 2018
Centinel Spine Announces STALIF C® Integrated Interbody(TM) Milestone Usage in Australia
Sep 26, 2018
Renovis Surgical Receives FDA Clearance for Tesera Trabecular Technology 3D-Printed Lateral Interbody Fusion System
Jul 18, 2018
Brazil Spinal Implants and VCF Market 2018-2024: Units Sold, Average Selling Prices, Procedure Volumes, Market Values, Shares, Product Pipeline & Forecasts
Jun 12, 2018
icotec AG Received FDA Clearance to Market BlackArmor® Carbon/PEEK Interbody Cages
May 14, 2018
Gait Trainer Market Will Hit at a CAGR of 4.9% From 2018 to 2028 - Future Market Insights
Feb 02, 2018
Spinal Implants and VCF Market Report Suite for Europe 2017-2023 - Unit Sales, ASPs, Market Value & Growth Trends
Feb 02, 2018
Brazil Minimally Invasive Spinal Implants Market Report 2018
Jan 04, 2018
NuVasive Extends First-Of-Its-Kind Porous PEEK Interbody To TLIF And PLIF Procedures
Aug 11, 2017
Renovis® Surgical Receives FDA Clearance for 3D-Printed Posterior Lumbar Interbody Fusion Systems
Jul 25, 2017
Vertera Spine Announces FDA Clearance of COALESCE(TM) porous PEEK Lumbar Interbody Fusion Device