WHITMORE ANKLE X-RAY EXTENSION (AXE)

WHITMORE ANKLE X-RAY EXTENSION (AXE) is an FDA 510(k)-cleared medical device (K933778) manufactured by Whitmore Ent., Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 12, 1993. Regulation: 8.