NuVasive Update on COALESCE, COHERE Interbody Fusion Devices
NuVasive launched COALESCE for Thoracolumbar Interbody Fusion, and announced FDA 510(k) clearance to market the COHERE® Cervical Interbody Fusion device with expanded indications....
NuVasive launched COALESCE for Thoracolumbar Interbody Fusion, and announced FDA 510(k) clearance to market the COHERE® Cervical Interbody Fusion device with expanded indications....
Initial outcomes from Zyga's EVSI study indicate a significant reduction in low back pain and opioid use in patients receiving...
Initial cases are complete and multiple surgeries performed with Life Spine’s SIMPACT™ Tri-Fin Sacroiliac Joint Fusion device, following its November 2017...
FH Orthopedics marked the sale of >6,000 units of its cervical and lumbar artificial discs, CP-ESP® and LP-ESP®....
K2M received approval under the CE Mark for its CAPRI® Cervical 3D Expandable Corpectomy Cage, and announced completion of its first surgical...
FDA’s Orthopaedic and Rehabilitation Devices Panel recommended against Premarket Approval of Intrinsic Therapeutics’ Barricaid Anular Closure for partial anulus replacement to...
Xenco Medical launched TraumaGP's, reportedly the first on-demand trauma surgery delivery app with real-time GPS driver tracking for disposable implant...
DePuy Synthes launched the CONCORDE™ Clear MIS discectomy device in EMEA regions....
Omnia Medical received FDA 510(k) clearance to market its PEEK-OPTIMA HA-based vertebral body replacement device....
Camber Spine received FDA 510(k) clearance to market the SPIRA™-C Open Matrix cervical interbody fusion device....
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