MX Orthopedics was awarded a state-backed US $0.75MM Accelerator Loan. Funds will support commercialization of dynaMX™ superelastic orthopaedic fracture fixation implants.
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.Â
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.
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.
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.
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.
Integra LifeSciences launched the Integra® Fin-Lockâ„¢ Glenoid for the Titanâ„¢ Modular Shoulder System to address glenoid component loosening and failure in total shoulder arthroplasty.Â
Interventional Spine announced FDA clearance of the 80 Lumbar Lordotic Opticageâ„¢, an intervertebral body fusion device for use with autogenous bone graft in patients with degenerative disc disease.Â
Implanet received FDA 510(k) clearance and CE Mark approval for the Jazz Claw®, a hybrid implant designed to treat degenerative spinal pathologies.