ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.

ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD. is an FDA 510(k)-cleared medical device (K933059) manufactured by Jace Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1994. Regulation: 8.