Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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