VERTEX® Reconstruction System
- Primary DI
- 00613994460707
- Brand
- VERTEX® Reconstruction System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 7751940
- Device description
- SCREW 7751940 4.5 X 40MM POSTED
- Published
- 2015-09-02
- 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 |
|---|---|
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K083071 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00613994460707 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00613994460707 | 00613994460707 | 613994460707 | 0613994460707 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone-screw internal spinal fixation system, non-sterile | An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 40 | Millimeter |
| Outer Diameter | 4.5 | 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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| 00763000857943 | T2 STRATOSPHERE™ Expandable Corpectomy System | 4361220 | 2026-06-01 | |
| 00763000857998 | T2 STRATOSPHERE™ Expandable Corpectomy System | 4361308 | 2026-06-01 | |
| 00763000881252 | Clydesdale™ Spinal System | 4986040 | 2026-05-29 | |
| 00199150073504 | Medtronic Reusable Instruments | EX1225001 | 2026-05-25 | |
| 00199150071685 | Medtronic Reusable Instruments | EX0226140 | 2026-05-24 | |
| 00199150071692 | Medtronic Reusable Instruments | EX0226150 | 2026-05-24 | |
| 00199150071708 | Medtronic Reusable Instruments | EX0226160 | 2026-05-24 | |
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| 00199150071753 | Medtronic Reusable Instruments | EX0226040 | 2026-05-24 | |
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