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Rti Surgical, Inc.

7 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Pre-Sutured Tendon (K253145)Rti Surgical, Inc.2025-10-22
Moldable Bone Void Filler and Moldable Bone Void Filler + CCC (K241555)Rti Surgical, Inc.2025-02-21
Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand ) (K230036)Rti Surgical, Inc.2023-06-23
Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D Technology (K172343)Rti Surgical, Inc.2017-10-23
Fortilink™-C with TETRAfuse™ 3D Technology (K163673)Rti Surgical, Inc.2017-05-23
FORTIVA PORCINE DERMIS, TUTOPLAST PORCINE DERMIS (K142070)Rti Surgical, Inc.2014-10-27
BOVINE PERICARDIUM SUTURABLE DURAL GRAFT, TUTOPATCH DM GRAFT, TUTOPLAST BOVINE PERICARDIUM DM (K132850)Rti Surgical, Inc.2014-03-31

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Every clearance here is in the API, with alerts when new ones post.