CONSTRUX - MINI PTC
- Primary DI
- 18257200030552
- Brand
- CONSTRUX - MINI PTC
- Company
- ORTHOFIX INC.
- Model
- 37-3013SP
- Device description
- 12mm L X 12mm W, 13mm H Lordotic Implant
- Published
- 2017-08-01
- Public version status
- Update
- 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 |
|---|
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 18257200030552 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|
| 18257200030552 | 18257200030552 |
GMDN Terms
| Term | Definition |
|---|
| Vertebral body prosthesis, non-sterile | A non-sterile implantable device designed to replace or repair (fuse) the spinal bony segments, or vertebrae, lost or injured as a consequence of, e.g., trauma, deformity, tumour, or degenerative disease. It is typically intended to be used with supplemental spinal fixation and may be used with a bone graft. It is usually made of metal, polymer, or a combination of these materials. This device must be sterilized prior to use. |
Device Sizes
| Type | Value | Unit |
|---|
| Height | 13 | Millimeter |
| Length | 12 | Millimeter |
| Width | 12 | Millimeter |
Regulatory Flags
- DUNS number
- 927083808
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- 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
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