Medicrea Gains FDA Clearance for 3D-Printed Ti Interbody
Medicrea received FDA 510(k) clearance to market IB3D™ 3D-printed interbody devices, and introduced its AdapTEK™ in-house additive manufacturing technology....
Medicrea received FDA 510(k) clearance to market IB3D™ 3D-printed interbody devices, and introduced its AdapTEK™ in-house additive manufacturing technology....
Life Spine commenced limited launch of the SIMPACT™ TRI-FIN sacroiliac joint fixation screw....
Highmark is reported to be the first and only private payor to issue exclusive positive coverage for Paradigm Spine’s coflex®...
Titan Spine entered the Australian market with its Endoskeleton® interbody fusion devices and surface technology....
SpineGuard and XinRong Medical are launching Classic PediGuard® pedicle screw placement tools in China....
Amedica made a (510)k submission to FDA for its Valeo C+CSC with Lumen cervical spinal implant....
Spineart announced completion of 1,000 U.S. surgeries with the standalone Scarlet® AC-T device....
Pinnacle Spine expects 4Q17 FDA 510(k) clearance to market InFill® Lateral Lumbar Fusion systems with Invibio’s HA Enhanced PEEK-OPTIMA material. ...
SAGICO commenced North American debut of its expandable interbody fusion system, comprising Aria Lumbar and Arion Cervical devices....
AxioMed introduced its lateral total disc replacement, for which first surgery completion is expected by year-end....
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