CD Horizon™ ModuLeX™ Spinal System
- Primary DI
- 00763000962500
- Brand
- CD Horizon™ ModuLeX™ Spinal System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 559200112
- Device description
- HEAD PK 559200112 5.5/6.0 CCM VOY MAS4PK
- Published
- 2025-03-30
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- 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 |
|---|---|
| K232141 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20763000962504 | Primary | GS1 | 0 | |
| 00763000962500 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20763000962504 | 20763000962504 | ||
| 00763000962500 | 00763000962500 | 763000962500 | 0763000962500 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal bone screw, non-bioabsorbable | A small, threaded, implantable rod with a screw head and drive intended for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 830350380
- Device count
- 4
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 00199150082803 | Medtronic Reusable Instruments | X0226025 | 2026-07-04 | |
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| 00199150082827 | Medtronic Reusable Instruments | X0226027 | 2026-07-04 | |
| 00199150082834 | Medtronic Reusable Instruments | X0226028 | 2026-07-04 | |
| 00199150082841 | Medtronic Reusable Instruments | X0226029 | 2026-07-04 | |
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| 00199150082865 | Medtronic Reusable Instruments | X0226031 | 2026-07-04 | |
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|---|---|---|---|---|
| 00643169465879 | MSB CD HORIZON Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-06-28 |
| 00643169101296 | MSB VERTEX® Reconstruction System | MEDTRONIC SOFAMOR DANEK, INC. | KWP | 2026-06-27 |
| 10889981441555 | VIRATA | Seaspine Orthopedics Corporation | KWP | 2026-06-24 |
| 10889981441609 | VIRATA | Seaspine Orthopedics Corporation | KWP | 2026-06-24 |
| 10889981441616 | VIRATA | Seaspine Orthopedics Corporation | KWP | 2026-06-24 |
| 10889981441623 | VIRATA | Seaspine Orthopedics Corporation | KWP | 2026-06-24 |
| 10889981441661 | VIRATA | Seaspine Orthopedics Corporation | KWP | 2026-06-24 |
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