Life Spine Receives FDA Clearance of PRO-LINK Ti Standalone Cervical Spacer
Life Spine received FDA 510(k) clearance to market the PRO-LINK® Ti Standalone Cervical Spacer. Full launch is scheduled for the end of...
Life Spine received FDA 510(k) clearance to market the PRO-LINK® Ti Standalone Cervical Spacer. Full launch is scheduled for the end of...
NuVasive Specialized Orthopedics received FDA 510(k) clearance to market the MAGEC® system for treatment of severe spinal deformity....
The ApiFix® system for correction of Adolescent Idiopathic Scoliosis has been used in 100 patients to date, at 12 sites in nine...
Meditech Spine received FDA 510(k) clearance to market CURE Anterior Cervical Plates to complement its Talos®-C (HA) interbody devices....
Progenerative Medical entered into a technology licensing agreement with Kinetic Concepts for exclusive, worldwide rights to IP and a preclinical...
Implanet announced initial positive results following use of the Jazz Lock® spinal implant in >25 cases. Full global launch is slated to...
Vexim received approval in Australia to market SpineJack® and the Masterflow™ cement delivery system. Product is slated for initial export within...
Implanet was granted a U.S. patent protecting the JAZZ® technology platform through 2032. ...
Life Spine announced successful completion of initial cases using the SENTRY™ Lateral Plate. Full launch will occur by the end of...
Tyber Medical commenced commercial launch of a low profile lateral plating system....
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