AxSOS 3 Ti - Stryker Plating System
FDA 510(k)FDA UDIEUDAMEDClass II (US FDA 510(k))
by Stryker GmbH
Identity
- Trade Name
- AXSOS EUDAMEDFDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDIOrthopaedic bone screw (non-sliding) FDA UDIInstrument tray, reusable FDA UDI
- Device Name
- AXSOS 3 INSTRUMENTS - TRAYS AND TRAY ACCESSORIES - CLASS I - NON STERILE EUDAMEDAXSOS 3 - SCREW - TITANIUM ALLOY - CLASS IIB - STERILE EUDAMEDAXSOS 3 - PLATE - TITANIUM ALLOY - CLASS IIB - STERILE EUDAMEDAXSOS - PLATE - STAINLESS STEEL - CLASS IIB - NON STERILE EUDAMEDDistal Medial Tibia Plate FDA UDIDistal Lateral Femur Plate TS FDA UDICortex Screw FDA UDIPlate Insert with tag Proximal Lateral Tibia FDA UDI
- Model / Reference
- 627444S EUDAMEDFDA UDI437514 EUDAMEDFDA UDI661750S EUDAMEDFDA UDI437534 EUDAMEDFDA UDI940152 EUDAMEDFDA UDI08858251002819TF EUDAMED08858251003123SA EUDAMED607485S EUDAMED08858251003098T4 EUDAMED08858251005293TJ EUDAMED
- Description
- Distal Medial Tibia Plate FDA UDIDistal Lateral Femur Plate TS FDA UDICortex Screw FDA UDIPlate Insert with tag Proximal Lateral Tibia FDA UDI
Identifiers
- Catalog Number
- 627444S FDA UDI437514 FDA UDI661750S FDA UDI437534 FDA UDI940152 FDA UDI
- Primary DI / UDI-DI
- 07613327082692 EUDAMEDFDA UDI07613154396139 EUDAMEDFDA UDI04546540686756 EUDAMEDFDA UDI07613154396276 EUDAMEDFDA UDI07613327089257 EUDAMEDFDA UDI07613252649502 EUDAMED
- Basic UDI-DI
- 08858251002819TF EUDAMED08858251003123SA EUDAMED08858251003098T4 EUDAMED08858251005293TJ EUDAMED
- Direct Marketing DI
- 07613327089257 EUDAMED
- FDA Product Code
- HRS FDA 510(k)FDA UDIHWC FDA UDILXH FDA UDI
- EMDN Code
- P091280 OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - ACCESSORIES EUDAMEDP09120601 CORTICAL SCREWS EUDAMEDP09120599 BONE FIXATION PLATES - OTHER EUDAMED
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable FDA UDIOrthopaedic bone screw (non-sliding) FDA UDIInstrument tray, reusable FDA UDI
- Models / Variants
- Stryker Plating System FDA 510(k)FDA UDIEUDAMED
Classification
- Device Class
- Class I EUDAMEDFDA UDIClass IIb EUDAMEDClass II FDA 510(k)FDA UDI
- Legislation / Framework
- 21 CFR Part 888.3030 FDA 510(k)
- Regulation Number
- 888.3030 FDA 510(k)FDA UDI888.3040 FDA UDI888.4540 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Reusable
No
Contains Latex
No
Reprocessed
No
Sutures
Yes
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Dimensions & Sizes
- Size
- Length — 227.0 Millimeter FDA UDILength — 310.0 Millimeter FDA UDILength — 50.0 Millimeter FDA UDI
The AxSOS 3 Ti; Stryker Plating System is a monoaxial locking plate designed for long bone fracture fixation. It features a titanium alloy construction with a patented screw-to-plate interface, enabling secure fixation through both locking and non-locking screws. This system is categorized under orthopedic plating devices and is intended for internal stabilization of fractures in long bones, such as the femur.
The device is supplied as a sterile, single-use system and is regulated under FDA 510(k) clearance (K162439) and MDR compliance. It includes streamlined instrumentation to facilitate efficient intraoperative use. The system is available in various configurations tailored for distal femur applications, with specific plate and screw sizes detailed in the accompanying technical documentation. Storage and handling follow standard sterile orthopedic implant protocols.
This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: AxSOS 3 Ti Plating - Stryker, AxSOS 3 Ti Distal Lateral Femur | Stryker, PDF AxSOS 3 Titanium Locking Plate System - Stryker MedEd
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Active |
| FDA 510(k) | United States | FDA_510K | K162439 | Class II | Active |
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Manufacturer
- Manufacturer
- Stryker GmbH
Sources (12)
- FDA 510(k) K162439 24 fields · synced Sep 30, 2026
- FDA UDI e18e3421-41dc-4046-8558-602e082a0bd2 35 fields · synced May 30, 2026
- FDA UDI c8cebf71-d5d8-4336-977b-c4d4fdf2e6f5 36 fields · synced May 30, 2026
- FDA UDI ab041c91-6759-40eb-b772-8fc3fb5ceaed 35 fields · synced May 30, 2026
- FDA UDI 92026ef9-e49e-4faa-b3e0-141b7848bbef 36 fields · synced May 30, 2026
- FDA UDI ecd395b3-1461-4bc3-8591-ac52788766d0 34 fields · synced May 30, 2026
- EUDAMED d3e4607a-38a2-487f-a75d-38ac391996fd 61 fields · synced Sep 17, 2026
- EUDAMED e6e01395-0d49-46ad-afb8-4145e983e5e3 61 fields · synced Sep 17, 2026
- EUDAMED 859409a4-f723-48bd-8fb8-7a4cf6857401 61 fields · synced Sep 30, 2026
- EUDAMED 817dc42c-4da8-4a22-b2b6-c0e902b9b82e 61 fields · synced Sep 30, 2026
- EUDAMED a546621f-75ec-4358-a688-534bb60487e7 61 fields · synced Sep 30, 2026
- EUDAMED 03b2086f-bad6-4059-b4bb-4bb6cf25ea29 61 fields · synced Sep 30, 2026