Klassic Blade Neck Trial, Standard
- Primary DI
- 00819251020435
- Brand
- Klassic Blade Neck Trial, Standard
- Company
- TOTAL JOINT ORTHOPEDICS, INC.
- Model
- 1110.02.000
- Device description
- Blade Neck Trial, Standard, size 4/5/6
- Published
- 2019-10-21
- 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
Product Codes
| Code | Name |
|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00819251020435 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Femoral stem prosthesis trial | A copy of a final femoral stem prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral head trial prostheses. It is typically made of metal or polymer material and includes trial stems, trial sleeves, and trial necks. This is a reusable device intended to be sterilized prior to use. |
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 HD Hip System should be stored in a clean, dry location at room
temperature |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | Email |
|---|
| +1(801)486-6070 | udi@tjoinc.com |
Regulatory Flags
- DUNS number
- 078416717
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- 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
- true
Other Devices From This Company
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|---|
| 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 |
| 00810094692674 | Klassic Knee Template, Tibial Baseplate, Revision | 2909.00.000 | | 2026-01-07 |
| 00810094692476 | Narrow Distal Femur Cut Block | SRI-10047 | | 2025-08-27 |
| 00810094692544 | Klassic ONE Universal Cone & Revision Baseplate Tray, Baseplate Insert | 2417.00.200 | | 2025-07-28 |
| 00810094692339 | Acetabular Reamer Adapter | SRI-10044 | | 2025-06-26 |
| 00810094691790 | Klassic Knee Templates, Stem Extensions | 2806.00.000 | | 2025-05-14 |
| 00810094692322 | Spline Wrench, Closed | 2017.00.100 | | 2025-05-14 |
| 00810094692346 | Intramedullary Reamer, Revision | 2026.10.000 | | 2025-05-14 |
| 00810094692353 | Intramedullary Reamer, Revision | 2026.11.000 | | 2025-05-14 |
| 00810094692360 | Intramedullary Reamer, Revision | 2026.12.000 | | 2025-05-14 |
| 00810094692377 | Intramedullary Reamer, Revision | 2026.13.000 | | 2025-05-14 |
| 00810094692384 | Intramedullary Reamer, Revision | 2026.14.000 | | 2025-05-14 |
| 00810094692391 | Intramedullary Reamer, Revision | 2026.15.000 | | 2025-05-14 |
| 00810094692407 | Intramedullary Reamer, Revision | 2026.16.000 | | 2025-05-14 |
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