Uni FB tibial component LL/RM
- Primary DI
- 04048844205331
- Brand
- Uni FB tibial component LL/RM
- Company
- implantcast GmbH
- Model
- 40100012
- Published
- 2021-01-12
- 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
Product Codes#
| Code | Name |
|---|---|
| HSX | Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HSX | Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K203341 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04048844205331 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04048844205331 | 04048844205331 | 4048844205331 |
GMDN Terms#
| Term | Definition |
|---|---|
| Uncoated unicondylar knee tibia prosthesis, metallic | A sterile implantable device designed to replace the bearing surface of one tibial condyle (tibial component) during primary or revision unicompartmental replacement of the knee joint. It is made of metal [e.g., cobalt-chrome (Co-Cr)] and is not coated with a material intended to improve fixation and stability. The device articulates with a femoral component and an insert, and its implantation is intended to be performed with bone cement. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 324369826
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04048844017309 | NA | 25862805 | 2026-06-02 | |
| 04048844708443 | EPORE® XO | 02208050 | 2026-06-02 | |
| 04048844711597 | EPORE® XO | 02208062 | 2026-06-02 | |
| 04048844711726 | EPORE® XO | 0220805800 | 2026-06-02 | |
| 04048844711740 | EPORE® XO | 0220806200 | 2026-06-02 | |
| 04048844711795 | EPORE® XO | 0220807200 | 2026-06-02 | |
| 04048844711870 | EPORE® XO | 02209056 | 2026-06-02 | |
| 04048844711917 | EPORE® XO | 0220904800 | 2026-06-02 | |
| 04048844711955 | EPORE® XO | 0220905600 | 2026-06-02 | |
| 04048844711979 | EPORE® XO | 02209060 | 2026-06-02 | |
| 04048844712020 | EPORE® XO | 0220906400 | 2026-06-02 | |
| 04048844712068 | EPORE® XO | 0220906800 | 2026-06-02 | |
| 04048844712099 | EPORE® XO | 02209072 | 2026-06-02 | |
| 04048844712723 | NA | 02563246 | 2026-06-02 | |
| 04048844712747 | NA | 02563654 | 2026-06-02 | |
| 04048844712761 | NA | 02563662 | 2026-06-02 | |
| 04048844712785 | NA | 02564054 | 2026-06-02 | |
| 04048844712808 | NA | 02564062 | 2026-06-02 | |
| 04048844712822 | NA | 02582842 | 2026-06-02 | |
| 04048844712846 | NA | 02583650 | 2026-06-02 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 05404028001257 | SurgiCase Planner | Materialise NV | HSX | 2026-05-28 |
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| 07613327127515 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2017-11-24 |
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| 07613327127560 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2017-11-24 |
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| 07613327049305 | Avon | Howmedica Osteonics Corp. | HSX | 2017-06-19 |
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| 07613327051179 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |
| 07613327051186 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |
| 07613327051193 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |
| 07613327051216 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |
| 07613327051223 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |
| 07613327051230 | INSTRUMENT | Howmedica Osteonics Corp. | HSX | 2016-09-24 |