200+ spine medtech FDA clearances in 2023
The Food and Drug Administration cleared more than 200 spine-related devices and technologies with 510(k) approval in 2023.
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The Food and Drug Administration cleared more than 200 spine-related devices and technologies with 510(k) approval in 2023.
Kleiner Device Labs earned a U.S. patent for its KG2 Surge flow-thru interbody system, the company said Oct. 9.
Dallas TX - Evolution Spine LLC is proud to announce the first implantation of the E3D-A™ Integrated ALIF cage by Dr. Mark Valente, DISC Spine Institute in Dallas TX. The E3D-A™ Interbody System received 510(k) clearance from the U. S. Food and Drug Administration (FDA) for its Integrated and
The demand analysis of Global Extreme Lateral Interbody Fusion (XLIF) Surgery Market size & share revenue was worth around $982.39 M in 2022 and is...
Dublin, May 12, 2023 (GLOBE NEWSWIRE) -- The "Microelectronic Medical Implants Global Market Report 2023" report has been added to ...