KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN

KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN is an FDA 510(k)-cleared medical device (K961522) manufactured by Synvasive Technology, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 22, 1996. Regulation: 8.