POLYMER OBL SB ANCHOR / SUTURE COMBINATION

POLYMER OBL SB ANCHOR / SUTURE COMBINATION is an FDA 510(k)-cleared medical device (K982996) manufactured by Orthopaedic Biosystems, Ltd.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 1999. Regulation: 8.