Rti Surgical, Inc. Dba Rti Biologics is one of 18426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rti Surgical, Inc. Dba Rti Biologics - FDA 510(k) Cleared Devices
Recent clearances: Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System, Interbody Fusion (IBF)/Vertebral Body Replacement(VBR) System
2
Total
2
Cleared
0
Denied
Rti Surgical, Inc. Dba Rti Biologics has 2 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rti Surgical, Inc. Dba Rti Biologics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rti Surgical, Inc. Dba Rti Biologics
2 devices