MX Orthopedics Secures $0.75MM Accelerator Loan
MX Orthopedics was awarded a state-backed US $0.75MM Accelerator Loan. Funds will support commercialization of dynaMX™ superelastic orthopaedic fracture fixation implants. May 31, 2016
Tyber Medical Enters Australia Market
Tyber Medical’s interbody spinal device line has been accepted into the Australian Registry of Therapeutic Goods. Private label partners are slated to launch products in 3Q16. May 31, 2016
Spine Wave Completes an $11MM Financing
Spine Wave closed a US $11MM round of new financing. Proceeds will fund the company’s largest product portfolio expansion to date. May 31, 2016
Ortho Kinematics Receives Health Canada Approval for Vertebral Motion Analysis
Ortho Kinematics received Health Canada approval for its lead product, Vertebral Motion Analysis, a diagnostic test for the assessment of spinal motion and radiographic instability. May 25, 2016
Acumed Launches Ankle Plating System 3
Acumed launched the Ankle Plating System 3, comprised of 7 plate families that span the lateral, medial, and posterior malleoli, and used in combination with the Acumed Small Fragment Base Set. May 25, 2016
Centinel Spine Expands MIDLINE II-Ti in U.S. and Australia
Centinel Spine expanded its MIDLINE II-Ti product family, a Ti-ACTIVE™ coated, No-Profile, anterior lumbar Integrated Interbody device, in the U.S. and Australia. May 24, 2016
Vertebral Technologies Announces Launch of InterLinkâ„¢ Pedicle Screw System
Vertebral Technologies launched the InterLink™ pedicle screw system, including 22 polyaxial pedicle screws, 19 spinal rods, cross-connectors and set screws, to be used for single or multiple level fixation. May 24, 2016
Integra LifeSciences Launches Fin-Lockâ„¢ Glenoid
Integra LifeSciences launched the Integra® Fin-Lock™ Glenoid for the Titan™ Modular Shoulder System to address glenoid component loosening and failure in total shoulder arthroplasty. May 24, 2016
Interventional Spine Announces FDA Clearance of Lordotic Opticageâ„¢
Interventional Spine announced FDA clearance of the 80 Lumbar Lordotic Opticage™, an intervertebral body fusion device for use with autogenous bone graft in patients with degenerative disc disease. May 24, 2016
Implanet Receives FDA Clearance and CE Mark for Jazz Claw Implant
Implanet received FDA 510(k) clearance and CE Mark approval for the Jazz Claw®, a hybrid implant designed to treat degenerative spinal pathologies. May 23, 2016
