iTotal Identity 3DP Porous Knee
- Primary DI
- 00840097515106
- Brand
- iTotal Identity 3DP Porous Knee
- Company
- Restor3d, Inc.
- Model
- PAT-012-3209
- Device description
- iTotal Identity 3DP Porous Round Patella 32mm x 9mm
- Published
- 2025-12-02
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- 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 |
|---|---|
| K243768 | 000 |
Premarket Details
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00840097515106 | Primary | GS1 | 0 |
GMDN Terms
| Term | Definition |
|---|---|
| Polyethylene patella prosthesis | An implantable device made of polyethylene (PE) intended to fully or partially replace the patella (kneecap) as part of a bicondylar knee joint replacement (primary or revision). It is designed to articulate with a prosthetic distal femoral component by attachment to the back of the natural patella with or without bone cement. |
Sterilization Methods
| Method |
|---|
Regulatory Flags
- DUNS number
- 080819836
- 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
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00840097534947 | Total Knee Instrumentation | 5201-1001 | 2025-10-10 | |
| 00840097534954 | Total Knee Instrumentation | 5201-1002 | 2025-10-10 | |
| 00840097534961 | Total Knee Instrumentation | 5201-1003 | 2025-10-10 | |
| 00840097513256 | Ossera™ AFX Instrumentation | 5740-0001 | 2025-12-18 | |
| 00840097513263 | Ossera™ AFX Instrumentation | 5740-0002 | 2025-12-18 | |
| 00840097513270 | Ossera™ AFX Instrumentation | 5740-0003 | 2025-12-18 | |
| 00840097513287 | Ossera™ AFX Instrumentation | 5740-3426 | 2025-12-18 | |
| 00840097515724 | Ossera™ AFX Instrumentation | 5740-3436 | 2025-12-18 | |
| 00840097515731 | Ossera™ AFX Instrumentation | 5740-3440 | 2025-12-18 | |
| 00840097519333 | Ossera™ AFX | 1740-3426 | 2025-12-18 | |
| 00840097519340 | Ossera™ AFX | 1740-3436 | 2025-12-18 | |
| 00840097519357 | Ossera™ AFX | 1740-3632 | 2025-12-18 | |
| 00840097519364 | Ossera™ AFX | 1740-3642 | 2025-12-18 | |
| 00840097519371 | Ossera™ AFX | 1740-4036 | 2025-12-18 | |
| 00840097519388 | Ossera™ AFX | 1740-4046 | 2025-12-18 | |
| 00840097532370 | Ossera™ AFX Instrumentation | 5740-3632 | 2025-12-18 | |
| 00840097532387 | Ossera™ AFX Instrumentation | 5740-3636 | 2025-12-18 | |
| 00840097533599 | Ossera™ AFX Instrumentation | 5741-2401 | 2025-12-18 | |
| 00840097533612 | Ossera™ AFX Instrumentation | 5741-3401 | 2025-12-18 | |
| 00840097533629 | Ossera™ AFX Instrumentation | 5741-3601 | 2025-12-18 |
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