VANGUARD COMPLETE KNEE SYSTEM
- Primary DI
- 00880304559660
- Brand
- VANGUARD COMPLETE KNEE SYSTEM
- Company
- Biomet Orthopedics, LLC
- Model
- 195770
- Catalog number
- 195770
- Published
- 2020-04-24
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00880304559660 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00880304559660 | 00880304559660 | 880304559660 | 0880304559660 |
GMDN Terms
| Term | Definition |
|---|
| Uncoated 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., cobalt-chrome (Co-Cr)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth; it includes a polyethylene (PE) insert/platform for femoral articulation. Device implantation is intended to be performed with bone cement. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
Regulatory Flags
- DUNS number
- 129278169
- 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
- false
Other Devices From This Company
Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|
| 00889024706774 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706781 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706798 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706804 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
| 00889024706811 | Biomet® | Biomet Orthopedics, LLC | JWH | 2026-03-12 |
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