Identity
- Trade Name
- Endo-Model SL Knee Prosthesis System FDA UDI
- Generic Name
- Uncoated knee tibia/insert prosthesis FDA UDI
- Device Name
- Proximal Tibial Replacement Components,modular, neutral FDA UDI
- Model / Reference
- 16-2849/25 FDA UDI
- Description
- Proximal Tibial Replacement Components,modular, neutral FDA UDI
Identifiers
- Catalog Number
- 16-2849/25 FDA UDI
- Primary DI / UDI-DI
- 04026575383375 FDA UDI
- 510(k) Number
- K151008 FDA UDI
- FDA Product Code
- KRO FDA UDILZO FDA UDIJDI FDA UDILWJ FDA UDI
- GMDN Term
- Uncoated knee tibia/insert prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3510 FDA UDI888.3353 FDA UDI888.3350 FDA UDI888.3360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Uncoated knee tibia/insert prosthesis
Endo-Model SL Knee Prosthesis System by WALDEMAR LINK GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Uncoated knee tibia/insert prosthesis.
- Arthrex® — Arthrex, Inc. · Class II
- Vanguard Complete Knee System — Biomet Orthopedics, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- LOSPA Total Knee System — Corentec Co., Ltd · Class II
- LOSPA Total Knee System — Corentec Co., Ltd · Class II
- LOSPA Modular Knee System — Corentec Co., Ltd · Class II
- Arthrex® — Arthrex, Inc. · Class II
- LOSPA Modular Knee System — Corentec Co., Ltd · Class II
Cleared under the same submission
K151008 also covers:
- Endo Model Knee Fusion Nail FK — WALDEMAR LINK GmbH & Co. KG
- Endo Model Knee Fusion Nail FK — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
- Endo-Model SL Knee Prosthesis System — WALDEMAR LINK GmbH & Co. KG
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- WALDEMAR LINK GmbH & Co. KG
Sources (1)
- FDA UDI 84053b00-25c3-4f8f-8d2b-a90be8822d68 35 fields · synced May 30, 2026