Regulacje i polityka gospodarcza · 18/11/1996

FDA Approves Spine-Tech's BAKSUPTM Interbody Fusion System

The U.S. Food and Drug Administration (FDA) has approved Spine-Tech, Inc.'s application for premarket approval of its BAKSUPTM Interbody Fusion System with instrumentation, following the recommendation of the Orthopedic and Rehabilitation Devices Panel. The FDA notified Spine-Tech of the approval on September 20, 1996.