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Rti Surgical, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories4
Latest FDA decision2025-10-22
TypeNumberDevice NameCodeDateActions
510(k) K253145 Pre-Sutured TendonGAT2025-10-22 View
510(k) K241555 Moldable Bone Void Filler and Moldable Bone Void Filler + CCCMQV2025-02-21 View
510(k) K230036 Pre-Sutured Tendon (4561SC / Single Strand); Pre-Sutured Tendon (4564SC / Quadruple Strand )GAT2023-06-23 View
510(k) K172343 Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D TechnologyMAX2017-10-23 View
510(k) K163673 Fortilink™-C with TETRAfuse™ 3D TechnologyODP2017-05-23 View
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