TRULIANT®
- Primary DI
- 10885862608147
- Brand
- TRULIANT®
- Company
- Exactech, Inc.
- Model
- 02-022-56-3545
- Catalog number
- 02-022-56-3545
- Device description
- Porous Tibial Tray without Screw Holes
- Published
- 2024-11-08
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
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 |
|---|---|
| K240393 | 000 |
Premarket Details
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10885862608147 | Primary | GS1 | 0 |
GMDN Terms
| Term | Definition |
|---|---|
| Trabeculated knee tibia/insert prosthesis | A sterile implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint or to replace a dysfunctional knee prosthesis (revision). It is made of metal (e.g., tantalum alloy) and has a convoluted/perforated surface intended to improve fixation and stability by promoting bone ingrowth; it also includes a polyethylene (PE) insert/platform for femoral articulation. Device implantation is typically intended to be performed without bone cement. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 157565946
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10885862609588 | Vantage | 351-21-23 | 351-21-23 | 2026-03-19 |
| 10885862639622 | AcuMatch | 103-00-01 | 103-00-01 | 2026-03-19 |
| 10885862648037 | Equinoxe | 313-01-38 | 313-01-38 | 2026-03-19 |
| 10885862648044 | Equinoxe | 313-01-41 | 313-01-41 | 2026-03-19 |
| 10885862648051 | Equinoxe | 313-01-44 | 313-01-44 | 2026-03-19 |
| 10885862648068 | Equinoxe | 313-01-47 | 313-01-47 | 2026-03-19 |
| 10885862648075 | Equinoxe | 313-01-50 | 313-01-50 | 2026-03-19 |
| 10885862648082 | Equinoxe | 313-01-53 | 313-01-53 | 2026-03-19 |
| 10885862648099 | Equinoxe | 313-05-01 | 313-05-01 | 2026-03-19 |
| 10885862648105 | Equinoxe | 313-05-02 | 313-05-02 | 2026-03-19 |
| 10885862648129 | Equinoxe | 313-07-01 | 313-07-01 | 2026-03-19 |
| 10885862648136 | Equinoxe | 313-07-02 | 313-07-02 | 2026-03-19 |
| 10885862648143 | Equinoxe | 313-07-03 | 313-07-03 | 2026-03-19 |
| 10885862648150 | Equinoxe | 313-07-05 | 313-07-05 | 2026-03-19 |
| 10885862648167 | Equinoxe | 313-07-07 | 313-07-07 | 2026-03-19 |
| 10885862648174 | Equinoxe | 313-07-10 | 313-07-10 | 2026-03-19 |
| 10885862648259 | Equinoxe | 313-25-38 | 313-25-38 | 2026-03-19 |
| 10885862648266 | Equinoxe | 313-25-41 | 313-25-41 | 2026-03-19 |
| 10885862648273 | Equinoxe | 313-25-44 | 313-25-44 | 2026-03-19 |
| 10885862648280 | Equinoxe | 313-25-47 | 313-25-47 | 2026-03-19 |
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