Klassic Tibial Insert, CR/Congruent, E-Link Poly
- Primary DI
- 00814703014055
- Brand
- Klassic Tibial Insert, CR/Congruent, E-Link Poly
- Company
- TOTAL JOINT ORTHOPEDICS, INC.
- Model
- 5302.02.016
- Device description
- Tibial Insert, CR/Congruent, E-Link Poly, size 2, 16mm
- Published
- 2018-03-29
- Public version status
- New
- 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#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K180159 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00814703014055 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00814703014055 | 00814703014055 | 814703014055 | 0814703014055 |
GMDN Terms#
| Term | Definition |
|---|---|
| Tibial insert | An implantable device designed to articulate the femoral and tibial components of a knee joint prosthesis during primary or revision bicondylar knee joint replacement. It is typically a one-piece contoured polyethylene (PE) insert, or a more complex device (e.g., a guide arm with a stem that is inserted into the tibial tray and a polymer glide) which will better reproduce the flexion of the knee joint due to its capacity for lateral rotation and anterior/posterior movement. This device is typically made of metal and/or a polymer. |
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 |
|---|
| Ethylene Oxide |
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
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00810094692698 | Modular Frog Eyes | 2263.00.000 | 2026-06-09 | |
| 00810094692704 | Distal Femoral Cut Block Connector | 2174.00.000 | 2026-06-09 | |
| 00810094692797 | Tibial Reamer, Square Tip, Klassic ONE 25/50mm | 2264.00.000 | 2026-06-09 | |
| 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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