RIALTO™ SI FUSION SYSTEM
- Primary DI
- 00643169273900
- Brand
- RIALTO™ SI FUSION SYSTEM
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 9000245
- Device description
- SCREW 9000245 SI TI CANN 12X45
- Published
- 2019-03-07
- 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 |
|---|---|
| OUR | Sacroiliac joint fixation |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OUR | Sacroiliac Joint Fixation | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K110472 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00643169273900 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00643169273900 | 00643169273900 | 643169273900 | 0643169273900 |
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 |
|---|---|---|
| Device Size Text, specify | 0 |
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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