SeaSpine Receives FDA 510(k) Clearance for Mariner Posterior Fixation

SeaSpine received FDA 510(k) clearance to market the Mariner™ Posterior Fixation pedicle screw system. Limited launch is underway, with full launch slated for 1H17.

Mariner features modular threaded technology and accompanying instrumentation, and is designed to reduce the number of trays needed for surgery. Other features include in situ modularity, motion limiting heads and rod versatility.

Source: SeaSpine Corporation