PREVISION HIP SYSTEM WITH RECON RING

PREVISION HIP SYSTEM WITH RECON RING is an FDA 510(k)-cleared medical device (K102424) manufactured by Aesculap Implant Systems, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 8, 2010. Regulation: 8.