Rti Surgical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Rti Surgical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Alachua, US.
Latest FDA clearance: Oct 2025. Active since 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rti Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Rti Surgical, Inc.
7 devices
Cleared
Oct 22, 2025
Pre-Sutured Tendon
Orthopedic
27d
Cleared
Feb 21, 2025
Moldable Bone Void Filler and Moldable Bone Void Filler + CCC
Orthopedic
266d
Cleared
Jun 23, 2023
Pre-Sutured Tendon (4561SC / Single Strand)
General & Plastic Surgery
178d
Cleared
Oct 23, 2017
Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D Technology
Orthopedic
82d
Cleared
May 23, 2017
Fortilink™-C with TETRAfuse™ 3D Technology
Orthopedic
147d
Cleared
Oct 27, 2014
FORTIVA PORCINE DERMIS, TUTOPLAST PORCINE DERMIS
General & Plastic Surgery
89d
Cleared
Mar 31, 2014
BOVINE PERICARDIUM SUTURABLE DURAL GRAFT, TUTOPATCH DM GRAFT, TUTOPLAST...
Neurology
201d