MODIFICATION TO MEDLINE STRIDER MIDI 3

MODIFICATION TO MEDLINE STRIDER MIDI 3 is an FDA 510(k)-cleared medical device (K042763) manufactured by Medline Industries, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 6, 2004. Regulation: 8.