P.L.U.S.®
- Primary DI
- 03663136017938
- Brand
- P.L.U.S.®
- Company
- SPINEVISION
- Model
- U1-S890T
- Device description
- TI 8.5mm X 90mm SCREW
- Published
- 2015-10-21
- 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
Related Records
Product Codes
| Code | Name |
|---|---|
| MNH | Orthosis, spondylolisthesis spinal fixation |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03663136017938 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03663136017938 | 03663136017938 | 3663136017938 |
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. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 390377518
- 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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|---|---|---|---|---|
| 03663136009308 | Hexanium® ACIF | AC2-A012-M11L | 2025-02-20 | |
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| 03663136009322 | Hexanium® ACIF | AC2-A012-M07L | 2025-02-20 | |
| 03663136009339 | Hexanium® ACIF | AC2-A012-M05L | 2025-02-20 | |
| 03663136009346 | Hexanium® ACIF | AC2-A012-S11L | 2025-02-20 | |
| 03663136009353 | Hexanium® ACIF | AC2-A012-S09L | 2025-02-20 | |
| 03663136009360 | Hexanium® ACIF | AC2-A012-S07L | 2025-02-20 | |
| 03663136009384 | Hexanium® ACIF | AC2-A012-L11C | 2025-02-20 | |
| 03663136009391 | Hexanium® ACIF | AC2-A012-L09C | 2025-02-20 | |
| 03663136009407 | Hexanium® ACIF | AC2-A012-L07C | 2025-02-20 | |
| 03663136009414 | Hexanium® ACIF | AC2-A012-L05C | 2025-02-20 | |
| 03663136009421 | Hexanium® ACIF | AC2-A012-M11C | 2025-02-20 | |
| 03663136009438 | Hexanium® ACIF | AC2-A012-M09C | 2025-02-20 | |
| 03663136009445 | Hexanium® ACIF | AC2-A012-M07C | 2025-02-20 | |
| 03663136009452 | Hexanium® ACIF | AC2-A012-M05C | 2025-02-20 | |
| 03663136009469 | Hexanium® ACIF | AC2-A012-S11C | 2025-02-20 | |
| 03663136009476 | Hexanium® ACIF | AC2-A012-S09C | 2025-02-20 | |
| 03663136009483 | Hexanium® ACIF | AC2-A012-S07C | 2025-02-20 | |
| 03663136009490 | Hexanium® ACIF | AC2-A012-S05C | 2025-02-20 | |
| 03663136009261 | Hexanium® ACIF | AC2-A012-L11L | 2025-02-19 |
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| 00763000887155 | CD HORIZON® Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MNH | 2026-03-16 |
| 00763000992033 | MSB CD HORIZON Spinal System | MEDTRONIC SOFAMOR DANEK, INC. | MNH | 2026-03-14 |
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