FDA 510(k) Applications Submitted by RTI SURGICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K172343 08/02/2017 Fortilink« Interbody Fusion (IBF) System with TETRAfuse« 3D Technology RTI Surgical, Inc.
K163673 12/27/2016 FortilinkÖ-C with TETRAfuseÖ 3D Technology RTI Surgical, Inc.
K132850 09/11/2013 BOVINE PERICARDIUM SUTURABLE DURAL GRAFT, TUTOPATCH DM GRAFT, TUTOPLAST BOVINE PERICARDIUM DM RTI SURGICAL, INC.
K142070 07/30/2014 FORTIVA PORCINE DERMIS, TUTOPLAST PORCINE DERMIS RTI SURGICAL, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact