T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System

FDA 510(k) K200880 · Stryker GmbH

Substantially Equivalent

510(k) numberK200880

Submission

Device name
T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System
Applicant
Stryker GmbH
Mahwah, NJ, US
Received
April 2, 2020
Decision date
July 1, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSB – Rod, Fixation, Intramedullary And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3020
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code HSB

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K261481Pangea Femur Reconstruction SystemHSB · Traditional Stryker GmbH06/29/2026SE
K261651Precice™ Max System and Precice™ Ankle Salvage SystemHSB · Special NuVasive Specialized Orthopedics06/18/2026SE
K253080AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)HSB · Traditional Suzhou and Science & Technology Development Corp.06/18/2026SE
K253155Fule Metallic Lockable Intramedullary Nail SystemsHSB · Traditional Beijing Fule Science & Technology Development…06/17/2026SE
K253046HERA Interlocking Intramedullary Nailing SystemHSB · Traditional ZheJiang Decans Medical Devices Co., Ltd.06/16/2026SE
K260146Fitbone® Transport and Lengthening SystemHSB · Traditional Orthofix Srl05/19/2026SE
K253991Fitbone™ Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAAHSB · Traditional Orthofix Srl05/08/2026SE
K261043AUTOBAHN™ Nailing SystemHSB · Special Globus Medical, Inc.04/24/2026SE
K252016Arthrex Humeral NailsHSB · Traditional Arthrex, Inc.03/20/2026SE
K252961Fusion FibFix NailHSB · Traditional Fusion Orthopedics USA, LLC03/18/2026SE

More from Fusion Orthopedics USA, LLC

510(k)DeviceDecision
K261481Pangea Femur Reconstruction SystemHSB · Traditional 06/29/2026SE
K253640T2 Alpha Femur Retrograde Nailing System; Pangea Femur Reconstruction SystemHSB · Traditional 02/03/2026SE
K253202Hoffmann LRF SystemKTT · Traditional 12/19/2025SE
K251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemHSB · Traditional 08/20/2025SE
K250163T2 Alpha Femur Retrograde Nailing SystemHSB · Traditional 08/13/2025SE
K242445Pangea Platform; Pangea Femur Plating System; Pangea Humerus Plating System; Pangea…HRS · Traditional 10/06/2024SE
K233919VariAx 2 Distal Radius SystemHRS · Traditional 03/25/2024SE
K233741Hoffmann LRF SystemKTT · Special 12/21/2023SE
K230045HipCheckQIH · Traditional 09/29/2023SE
K2318541788 4K Camera System with Advanced Imaging Modality; L12 LED Light Source with AIMOWN · Traditional 09/20/2023SE

Questions and answers

When was T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System cleared by the FDA?

T2 Tibial Nailing System, T2 Femoral Nail System, T2 Supracondylar Nail System, T2 Recon Nail System, T2 Greater Trochanter Nail (GTN),T2 Ankle Arthrodesis Nail,T2 Arthrodesis Nail System (K200880) received a 510(k) decision of Substantially Equivalent on July 1, 2020, 90 days after the submission was received.

What is the product code of K200880?

The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.