Duracon
- Primary DI
- 04546540319364
- Brand
- Duracon
- Company
- Howmedica Osteonics Corp.
- Model
- 6642-9-613
- Catalog number
- 6642-9-613
- Device description
- Constrained Tibial Insert
- Published
- 2015-09-24
- 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 |
|---|---|
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
| JDL | Prosthesis, hip, semi-constrained (metal cemented acetabular component) |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | Orthopedic | 2 |
| JDL | Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) | Orthopedic | 3 |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | Orthopedic | 2 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K964655 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04546540319364 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04546540319364 | 04546540319364 | 4546540319364 |
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 | |
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 058311945
- Device count
- 1
- Lot or batch
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04546540035523 | Omnifit | 2041C-2240 | 2041C-2240 | 2015-09-24 |
| 04546540035714 | Omnifit | 2041C-2846 | 2041C-2846 | 2015-09-24 |
| 04546540035790 | Omnifit | 2041C-3250 | 2041C-3250 | 2015-09-24 |
| 04546540035806 | Omnifit | 2041C-3254 | 2041C-3254 | 2015-09-24 |
| 04546540035813 | Omnifit | 2041C-3258 | 2041C-3258 | 2015-09-24 |
| 04546540035820 | Omnifit | 2041C-3262 | 2041C-3262 | 2015-09-24 |
| 04546540035837 | Omnifit | 2041C-3266 | 2041C-3266 | 2015-09-24 |
| 07613327016772 | UHR | UH1-36-22 | UH1-36-22 | 2015-09-24 |
| 07613327016789 | UHR | UH1-38-22 | UH1-38-22 | 2015-09-24 |
| 07613327016796 | UHR | UH1-40-22 | UH1-40-22 | 2015-09-24 |
| 07613327016802 | UHR | UH1-41-26 | UH1-41-26 | 2015-09-24 |
| 07613327016819 | UHR | UH1-41-22 | UH1-41-22 | 2015-09-24 |
| 07613327016826 | UHR | UH1-42-26 | UH1-42-26 | 2015-09-24 |
| 07613327016833 | UHR | UH1-42-22 | UH1-42-22 | 2015-09-24 |
| 07613327016840 | UHR | UH1-43-22 | UH1-43-22 | 2015-09-24 |
| 07613327016857 | UHR | UH1-42-28 | UH1-42-28 | 2015-09-24 |
| 07613327016864 | UHR | UH1-43-26 | UH1-43-26 | 2015-09-24 |
| 07613327016871 | UHR | UH1-44-22 | UH1-44-22 | 2015-09-24 |
| 07613327016888 | UHR | UH1-44-26 | UH1-44-26 | 2015-09-24 |
| 07613327016895 | UHR | UH1-44-28 | UH1-44-28 | 2015-09-24 |
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