VERTE-STACK® Spinal System
- Primary DI
- 00613994657114
- Brand
- VERTE-STACK® Spinal System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- X0709300
- Device description
- STRUT X0709300 CAPSTONE CENTER 17X58X22
- Published
- 2015-06-26
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MQP | Spinal Vertebral Body Replacement Device | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K041556 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00613994657114 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00613994657114 | 00613994657114 | 613994657114 | 0613994657114 |
GMDN Terms#
| Term | Definition |
|---|---|
| Metallic spinal interbody fusion cage | A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 22 | Millimeter |
| Outer Diameter | 17 | Millimeter |
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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| 00199150072057 | Medtronic Reusable Instruments | X6550023 | 2026-05-23 | |
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| 08033726407923 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-16 |
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| 08033726407701 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407718 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407725 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407732 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407749 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407756 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407763 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407770 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407787 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407794 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407800 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407817 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407824 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407831 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407848 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407855 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407862 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407879 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726407886 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
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| 08033726407916 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |
| 08033726408029 | DSC | SINTEA PLUSTEK SRL | MQP | 2015-10-09 |