Charlotte, N.C.-based Intelligent Implant Systems received U.S. FDA 510(k) clearance for its Marauder cervical-thoracic spine system.
TYRX announced that it has received FDA clearance for marketing the AIGISRx N Antibacterial Envelope for use with spinal cord neuromodulators.
San Diego-based NuVasive‘s anterior column realignment device for anterior lumbar interbody fusion launched in the U.S.
Maetta Sciences announced that it has received FDA clearance for a cobalt chrome orthopedic implantable device manufactured using its proprietary metal injection molding technology.
Aurora Spine was granted FDA 510(k) clearance for its ZIP minimally invasive interspinous fusion system.
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