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...

document icon

You are out of free articles for this month

Subscribe as a Guest for $0 and unlock a total of 5 articles per month.

You are out of five articles for this month

Subscribe as an Executive Member for access to unlimited articles, THE ORTHOPAEDIC INDUSTRY ANNUAL REPORT and more.

JV

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



Contact Us

0