MODIFICATION TO STRYKER BIOABSORBABLE INTERFERENCE SCREW SYSTEM

MODIFICATION TO STRYKER BIOABSORBABLE INTERFERENCE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K033252) manufactured by Stryker Endoscopy. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 2003. Regulation: 8.