MicroPort Orthopedics Receives FDA 510k Approval for Reindeer™ Locking Plate System

On March 29th, 2012, MicroPort Orthopedics Co., Ltd. announced the FDA 510k approval for its ReindeerTM Locking Plate System with registration Num. K112798, which is the first FDA approval product for MicroPort.
Corresponding to the BO (Bio-logical osteosynthesis) criterion, the newly approved locking plate system, combined with locking plate and locking bone screws, was designed for internal fixation of fracture for appendicular skeletons, which possesses unprecedented advantage for fixing complicated fracture and further potential applications. Since this is the first FDA approval for MicroPort orthopedics product following its CE certification, it has created favorable conditions for MicroPort to further explore the international market.