FLEXIBLE PHASED ARRAY SPINE COIL

FLEXIBLE PHASED ARRAY SPINE COIL is an FDA 510(k)-cleared medical device (K960497) manufactured by Philips Medical Systems (Cleveland), 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 July 4, 1996. Regulation: 8.