SOLUM IV BONE VOID FILLER

SOLUM IV BONE VOID FILLER is an FDA 510(k)-cleared medical device (K132470) manufactured by Spinesmith Partners, Llp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 2014. Regulation: 8.