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  Global Orthopedic Newsletter
  March 2018
 
Feature Story:

iData at AAOS 2018

The annual AAOS Conference provides a platform for key players in the orthopedics market to showcase products, demonstrate techniques, or present research to a targeted audience. At this year's conference, iData will be offering live demos of our new orthopedic research and market monitoring service, MedTrack. We are also running a global Orthopedic Surgeon Survey at the show. Please stop by, we would love to meet you in person.

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Orthofix Announces 510(k) Clearance and US Limited Market Launch of FORZA XP Expandable Spacer System

Orthofix International N.V., a global medical device company focused on musculoskeletal healing products, announced the 510(k) clearance and U.S. limited market launch of the FORZA® XP Expandable Spacer System. Designed to restore normal disc height in patients suffering from degenerative disc disease, the FORZA XP Expandable Spacer System can be expanded after insertion into the disc space in order to fit the patient’s anatomy. Made primarily of titanium alloy, these expandable interbodies are used for PLIF (Posterior Lumbar Interbody Fusion) and TLIF (Transforaminal Lumbar Interbody Fusion) procedures. Unlike the incremental expansion offered by some expandable interbody devices, the Orthofix System allows for...

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Zimmer Biomet Wins FDA Nod for Sidus Stem-Free Shoulder System

Zimmer Biomet announced that it won FDA clearance for its Sidus stem-free shoulder system. The newly cleared Sidus system is designed as a total shoulder arthroplasty solution for patients with good bone stock with either osteoarthritis, post-traumatic arthrosis, focal avascular necrosis of the humeral head or those who’ve had previous surgeries of the shoulder that don’t compromise fixation, the Warsaw, Ind.-based company said. “The Sidus stem-free shoulder system offers a novel approach to total shoulder arthroplasty requiring minimal bone resection. The Sidus system is designed to reduce...

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Polymer Bone Graft Substitute Receives FDA Clearance

Biotechnology startup Molecular Matrix Inc. has received 510(k) FDA clearance for a carbohydrate-based polymer that can help injured bones heal and regrow, reports the University of California, Davis, on its website. Osteo-P is a synthetic bone graft substitute that supports and guides the growth of new bone and is resorbed and replaced with the patients’ own bone during the healing process. Charles Lee, the founder of Molecular Matrix and also an assistant adjunct professor in the Department of Cell Biology and Human Anatomy at the UC Davis School of Medicine, expects to bring the biomaterial to...

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Zimmer Biomet APS Kit Offers Better Pain Relief For Knee Osteoarthritis

Zimmer Biomet Holdings, Inc. announced in a recent press release the results from the PROGRESS II Trial on the safety and efficacy of autologous protein solution prepared with its nStride APS Kit for treating osteoarthritis (OA) of the knee. The study titled “Clinical Outcomes of Knee Osteoarthritis Treated With an Autologous Protein Solution Injection: A 1-Year Pilot Double-Blinded Randomized Controlled Trial”, which originally appeared in The American Journal of Sports Medicine in October 2017, showed that solutions prepared with the kit offer significant improvement in pain, and has a comparable safety to saline. In this prospective, randomized, double-blind, saline-controlled pilot study, the researchers...

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Latest Publications

 
 

Mexico Market Report Suite For Minimally Invasive Spinal Implants 2018 - MedSuite

Brazil Market Report Suite For Minimally Invasive Spinal Implants 2018 - MedSuite

Argentina Market Report Suite For Minimally Invasive Spinal Implants 2018 - MedSuite

US Market Report Suite for Video and Integrated Operating Room Equipment 2018 – MedSuite

US Market Report Suite for Vascular Access Devices and Accessories 2018 – MedSuite

US Market Report Suite for Digital Dentistry Devices 2018 – MedSuite

US Market Report Suite for Infusion Therapy Devices 2018 – MedSuite

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Upcoming Publications

 
 

Europe Market Report Suite For Soft Tissue Reinforcement And Regeneration 2018 - MedSuite

Mexico Market Report Suite For Spinal Implants and VCF Devices 2018 - MedSuite

Argentina Market Report Suite For Spinal Implants and VCF Devices 2018 - MedSuite

US Market Report Suite For Interventional Cardiology Devices 2018 - MedSuite

Brazil Market Report Suite For Spinal Implants And Vertebral Compression Fracture Devices 2018 - MedSuite

 
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