DePuy Synthes Gains FDA 510(k) for TELIGEN Digital Tools

DePuy Synthes TELIGEN System Tower

DePuy Synthes was granted FDA 510(k) clearance to market the TELIGEN™ System, an integrated technology platform that supports minimally invasive surgical transforaminal lumbar interbody fusion (MIS-TLIF) procedures through digital tools for visualization and access.

TELIGEN will be available in the U.S. later this year.

TELIGEN comprises a...

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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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