HEYER-SCHULTE SPINAL CYST CATHETER/MODIFICATION

HEYER-SCHULTE SPINAL CYST CATHETER/MODIFICATION is an FDA 510(k)-cleared medical device (K905860) manufactured by Baxter Healthcare Corp. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 9, 1991. Regulation: 8.