Klassic Femur with Cobalt 3D, size 3
- Primary DI
- 00814703013485
- Brand
- Klassic Femur with Cobalt 3D, size 3
- Company
- TOTAL JOINT ORTHOPEDICS, INC.
- Model
- 5102.03.000
- Published
- 2016-10-31
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MBH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MBH | Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K162256 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00814703013485 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00814703013485 | 00814703013485 | 814703013485 | 0814703013485 |
GMDN Terms#
| Term | Definition |
|---|---|
| Coated knee femur prosthesis | A sterile implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr)] and is coated with a material (e.g., beads, hydroxyapatite, mesh) intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation may be performed with or without bone cement. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | The Klassic Knee System should be stored in a clean, dry location at room temperature |
| Special Storage Condition, Specify | 0 | 0 | The Klassic Knee System should be stored in a clean, dry location at room temperature |
Sterilization Methods#
| Method |
|---|
| Radiation Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(801)486-6070 | udi@tjoinc.com |
Regulatory Flags#
- DUNS number
- 078416717
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
- Sterilization required before use
- true
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|---|---|---|---|---|
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| 00810094692933 | Magnet Spacer, 5mm | 2027.00.000 | 2026-06-09 | |
| 00810094692940 | AP Sizer with Short Legs | SRI-10050 | 2026-05-15 | |
| 00810094692728 | CR Femoral Trial, Grit Blasted | SRI-10051.01 | 2026-02-05 | |
| 00810094692735 | CR Femoral Trial, Grit Blasted | SRI-10051.02 | 2026-02-05 | |
| 00810094692742 | CR Femoral Trial, Grit Blasted | SRI-10051.03 | 2026-02-05 | |
| 00810094692759 | CR Femoral Trial, Grit Blasted | SRI-10051.04 | 2026-02-05 | |
| 00810094692766 | CR Femoral Trial, Grit Blasted | SRI-10051.05 | 2026-02-05 | |
| 00810094692773 | CR Femoral Trial, Grit Blasted | SRI-10051.06 | 2026-02-05 | |
| 00810094692780 | CR Femoral Trial, Grit Blasted | SRI-10051.07 | 2026-02-05 | |
| 00810094692506 | Tibial Broach Impactor, Revision | 2904.00.000 | 2025-05-14 | |
| 00810094692278 | Universal Cone Impactor Head | 2021.12.012 | 2025-04-24 | |
| 00810094692285 | Universal Cone Impactor Head | 2021.34.018 | 2025-04-24 | |
| 00810094692292 | Universal Cone Impactor Head | 2021.57.024 | 2025-04-24 | |
| 00810094691950 | Universal Cone Impactor Head, Size 1, 12° | 2021.01.012 | 2024-09-06 | |
| 00810094691967 | Universa Cone Impactor Head, Size 2, 12° | 2021.02.012 | 2024-09-06 | |
| 00810094691974 | Universal Cone Impactor Head, Size 3, 18° | 2021.03.018 | 2024-09-06 | |
| 00810094691981 | Universal Cone Impactor Head, Size 4, 18° | 2021.04.018 | 2024-09-06 |
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