OSCILLATING BONE SAW BLADE, 6200 SERIES

OSCILLATING BONE SAW BLADE, 6200 SERIES is an FDA 510(k)-cleared medical device (K934390) manufactured by Boehringer Laboratories. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 25, 1994. Regulation: 8.