JuggerStitch Meniscal Repair Device

JuggerStitch Meniscal Repair Device is an FDA 510(k)-cleared medical device (K150424) manufactured by Biomet Manufacturing Corp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 14, 2015. Regulation: 8.