VANTAGE™ Anterior Fixation System
- Primary DI
- 00721902705427
- Brand
- VANTAGE™ Anterior Fixation System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 9330002
- Device description
- STAPLE 9330002 THORACIC CAUDAL TI
- Published
- 2015-07-31
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K023797 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00721902705427 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00721902705427 | 00721902705427 | 721902705427 | 0721902705427 |
GMDN Terms#
| Term | Definition |
|---|---|
| Metallic spinal fusion cage, non-sterile | A non-sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) made of metal [usually titanium (Ti)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for therapeutic spinal bone fusion to occur. Disposable devices associated with implantation may be included. This device must be sterilized prior to use. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 830350380
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
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