30 Day Trial

First Surgeries with Medacta MySpine Low Profile Guide Following FDA Clearance

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Medacta completed initial U.S. surgeries using its proprietary 3D-printed MySpine Patient Matched Technology Low Profile Guide, following its recent FDA clearance.

The Low Profile Guide supports identification of pedicle entry points, screw trajectories and implant specifications to potentially increase accuracy and outcomes. Further, it offers lowers exposure for a less invasive approach for degenerative and deformity surgeries of the thoracic and lumbar regions. 

First U.S. surgeries with the original iteration of MySpine technology occurred in 2014.

Sources: Medacta; ORTHOWORLD Inc.