MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL

MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDL is an FDA 510(k)-cleared medical device (K854420) manufactured by Meadox Surgimed, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 21, 1985. Regulation: 8.