SpineGuard Receives FDA 510(k) Clearance for Miniaturized and Directional Versions of Its Pediguard® Platform

Business Wire
SpineGuard Receives FDA 510(k) Clearance for Miniaturized and Directional Versions of Its Pediguard® Platform
New PediGuard(R) products designed to enhance pedicle screw penetration of small and/or difficult-to-access pedicles (Photo: Business Wire) Multimedia Gallery URL
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