CarboClear Lumbar Cage System
- Primary DI
- 07290110206864
- Brand
- CarboClear Lumbar Cage System
- Company
- CARBOFIX ORTHOPEDICS LTD
- Model
- Implant Trial-10x23x12mm
- Catalog number
- CCLC02312
- Device description
- A surgical tool for use with the lumbar intervertebral body fusion device (cage).The Implant Trial is intended for use before insertion of the implant into the intervertebral space, to assist in selection of correct implant dimensions and to verify implant position within the disc space.
- Published
- 2020-05-28
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K193378 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07290110206864 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07290110206864 | 07290110206864 | 7290110206864 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal implant trial | A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 1-800-408-0120 | usa@carbo-fix.com |
| +97299511511 | info@carbo-fix.com |
Regulatory Flags#
- DUNS number
- 649185170
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
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