POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM

POSTERIOR CERVICAL SPINE SURFACE COIL M1085AM is an FDA 510(k)-cleared medical device (K884369) manufactured by General Electric Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 27, 1988. Regulation: 8.