K2M Receives CE Mark for CAPRI Cervical 3D Expandable Cage
K2M received approval under the CE Mark for its CAPRI® Cervical 3D Expandable Corpectomy Cage, and announced completion of its first surgical...
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....
ChoiceSpine announced the first clinical use of the HAWKEYE® Ti vertebral body replacement, its first FDA-cleared, 3D-printed, titanium spinal fusion device....
Results of seven-year clinical trial follow-up indicate superiority of Globus Medical’s SECURE-C® cervical disc vs. ACDF in the treatment of cervical disc disease....
K2M announced completion of 300 surgical cases using the RHINE™ Cervical Disc....
Emerging Implant Technologies announced completion of first U.S. procedures with its 3D-printed titanium spinal cages. ...
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