Precision Spine Receives FDA 510(k) Clearance for AccuFit Lateral Plate

Precision Spine has received FDA 510(k) clearance for the AccuFit® Lateral Plate.

The titanium-based, low-profile AccuFit plate features four points of fixation and five sizes matched to the heights of ShurFit® LLIF Interbody cages. AccuFit is designed for use with the MD-Vue™ Lateral Access retractor, which Precision Spine debuted in 3Q16.

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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