CD HORIZON® Spinal System
- Primary DI
- 00613994124005
- Brand
- CD HORIZON® Spinal System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 7573730
- Device description
- SCREW 7573730 CANN FA 7.5X30 TI
- Published
- 2015-09-17
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes
| Code | Name |
|---|
| NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| NQP | Posterior Metal/Polymer Spinal System, Fusion | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00613994124005 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00613994124005 | 00613994124005 | 613994124005 | 0613994124005 |
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 | 30 | Millimeter |
| Outer Diameter | 7.5 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 830350380
- Device count
- 1
- DM exempt
- false
- 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
- true
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