MEDPOR SURGICAL GRANULE IMPLANTS

MEDPOR SURGICAL GRANULE IMPLANTS is an FDA 510(k)-cleared medical device (K982040) manufactured by Porex Surgical, Inc.. 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 7, 1998. Regulation: 8.