LUMIS™
- Primary DI
- 03663136006925
- Brand
- LUMIS™
- Company
- SPINEVISION
- Model
- MS1-M535T
- Device description
- MULTI-AXIAL SCREW, DIAMETER 5.5mm, LENGTH 35mm
- Published
- 2015-10-15
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Orthopedic | 2 |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Orthopedic | 2 |
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | Orthopedic | 2 |
| MNI | Orthosis, Spinal Pedicle Fixation | Orthopedic | 2 |
| NKB | Thoracolumbosacral Pedicle Screw System | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K112607 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03663136006925 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03663136006925 | 03663136006925 | 3663136006925 |
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
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 03663136001869 | C3® ACPS | C1-P1 0265 | 2015-10-15 | |
| 03663136001876 | C3® ACPS | C1-P1 0265N1 | 2015-10-15 | |
| 03663136001883 | C3® ACPS | C1-P1 0290 | 2015-10-15 | |
| 03663136001913 | C3® ACPS | C1-P1 0315N1 | 2015-10-15 | |
| 03663136001944 | C3® ACPS | C1-P1 0365 | 2015-10-15 | |
| 03663136002095 | C3® ACPS | C1-P2 0540N1 | 2015-10-15 | |
| 03663136002170 | C3® ACPS | C1-P3 0690 | 2015-10-15 | |
| 03663136002262 | C3® ACPS | C1-P4 0890 | 2015-10-15 | |
| 03663136002309 | C3® ACPS | C1-P4 1050 | 2015-10-15 | |
| 03663136019482 | C3® ACPS | C1-L1 0390 | 2015-10-15 | |
| 03663136019574 | C3® ACPS | C1-L3 0570 | 2015-10-15 | |
| 03663136001821 | C3® ACPS | C1-P1 0215 | 2015-10-15 | |
| 03663136001838 | C3® ACPS | C1-P1 0215N1 | 2015-10-15 | |
| 03663136001845 | C3® ACPS | C1-P1 0240 | 2015-10-15 | |
| 03663136001852 | C3® ACPS | C1-P1 0240N1 | 2015-10-15 | |
| 03663136001890 | C3® ACPS | C1-P1 0290N1 | 2015-10-15 | |
| 03663136001920 | C3® ACPS | C1-P1 0340 | 2015-10-15 | |
| 03663136001937 | C3® ACPS | C1-P1 0340N1 | 2015-10-15 | |
| 03663136001951 | C3® ACPS | C1-P1 0365N1 | 2015-10-15 | |
| 03663136001968 | C3® ACPS | C1-P1 0390 | 2015-10-15 |
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