5.5 MIS Spinal System II Instrument Set
5.5 MIS Spinal System II Instrument Set
Precio habitual
$2,079.00 USD
Precio de venta
$2,079.00 USD
Precio habitual
Envío calculado al finalizar la compra.
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5.5 MIS Spinal System II Pedicle Screw Instrument Set
Sterilized (Ethylene Oxide)
ISO 13485 Certified
CNAS Laboratory Accreditation
CE / TUV Compliant
A comprehensive, premium-grade instrument set meticulously engineered for Minimally Invasive Surgery (MIS) spinal fusion procedures. This specialized kit provides orthopedic surgeons with maximum precision, stability, and streamlined workflow control during advanced pedicle screw placement.
✨ Three Core Clinical Advantages
- Minimally Invasive: Truly percutaneous and minimally invasive approach, resulting in minimized incisions, minimal intraoperative bleeding, and rapid postoperative recovery.
- Versatile Distraction: Incorporates multiple distraction methods to enable highly effective and adaptable intraoperative spreading.
- High Clinical Outcomes: Documented high patient satisfaction, exceptionally low complication rates, and strong clinical adoption worldwide.
🛠️ Advanced Feature Details
- Long-Tab Reduction Instrument: Delivers robust support and structural stability required for smooth vertebral distraction and compression.
- Counter Torque Wrench: Effectively prevents screw rotation during final rod tightening, protecting the surrounding bone structure from excessive torque stresses.
- Expansion Sleeve: Facilitates gentle soft tissue dilation, protects critical surrounding anatomy, and guides accurate pedicle screw insertion.
- Precision Awl: Creates a perfectly centered initial pilot hole in the pedicle cortex, ensuring an accurate entry point.
- Compression-Distraction Forceps: Optimized mechanical advantages to compress or distract pedicle screws seamlessly, facilitating disc height restoration and precise cage placement.
🔬 Clinical Indications
| Minimally Invasive Lumbar Fusion Procedures | Lumbar Degenerative Pathologies Requiring Stabilization |
|---|---|
| MIS-TLIF / UBE-TLIF / PE-TLIF | Stenosis with Instability |
| PLIF / TLIF | Low-grade Spondylolisthesis (Grade I – II) |
| Percutaneous Lumbar Fusion | Disc Disease with Instability |
| OLIF (Oblique Lumbar Interbody Fusion) | - |
📦 Instrument Configuration List
| No. | Product Code | Description | Qty |
|---|---|---|---|
| 1 | RQ5JW2MTZ8 | φ8 Countersink Drill | 1 |
| 2 | RQ5JW2NTDZ15400 | Nitinol Guide Pin | 4 |
| 3 | RQ5JW2KSZ50 | φ5.0 Tap (hollow) | 1 |
| 4 | RQ5JW2KSZ60 | φ6.0 Tap (hollow) | 1 |
| 5 | RQ5JW2KSZ70 | φ7.0 Tap (hollow) | 1 |
| 6 | RQ5JW2SDQW | Screwdriver (Polyaxial) | 1 |
| 7 | RQ5JW2SDQD | Screwdriver (Monoaxial) | 1 |
| 8 | RQ5JW2DKTT | Counter Sleeve | 1 |
| 9 | RQ5JW2KZTT | Expansion Sleeve | 1 |
| 10 | RQ5JW2KSB | Hollow Quick Coupling Handle | 2 |
| 11 | RQ5JW2DWZDQ | Screw Tab Breaker | 1 |
| 12 | RQ5JW2SW4 | SW4.0 Screwdriver Shaft | 1 |
| 13 | RQ5JW2CDQZ | Torx Holding Screwdriver | 1 |
| 14 | RQ5JW2ZSJQZ | Screwdriver for Screw Nut | 1 |
| 15 | RQ5JW2CCQ | Awl | 2 |
| 16 | RQ5JW2ZBQC | Rod Inserter (long) | 1 |
| 17 | RQ5JW2ZBQD | Rod Inserter (short) | 1 |
| 18 | RQ5JW2SW4G | SW4.0 Hex Screwdriver | 1 |
| 19 | RQ5JW2FWQA | Reduction Screw Repositor A | 2 |
| 20 | RQ5JW2FWQB | Reduction Screw Repositor B | 2 |
| 21 | RQ5JW2FWTT | Reduction Sleeve | 1 |
| 22 | RQ5JW2TLFWQ | Traction Repositor | 1 |
| 23 | RQ5JW2CJQ | Distraction Compressor | 1 |
| 24 | RQ5JW2YSQ | Compressor | 1 |
| 25 | RQ5JW2CKQ | Spreader | 1 |
| 26 | RQ5JW2WBQ | Rod Bender | 1 |
| 27 | RQ5JW2XYDWB | Guide Plate | 1 |
| 28 | RQ5JW2LBQ | Rod Measuring Pliers | 1 |
| 29 | RQ5JW2MJHL | Instrument Box | 1 |
🔗 Related Product Recommendations
MIS Polyaxial Pedicle Screw
5.5 MIS Spinal System II Pedicle Screw
MIS 5.5 System Cement-Augmented Fenestrated Screw
📄 Ordering & Supply Specifications
- Sterilization State: Supplied in a pre-sterilized condition utilizing validated Ethylene Oxide (EO) sterilization cycles. Ready for immediate operating room integration if the packaging integrity is uncompromised.
- System Compatibility: Explicitly optimized for integration with the 5.5mm MIS Spinal System portfolio. Use with unapproved third-party implants is strictly discouraged.
- Storage Requirements: Store in a cool, dry, well-ventilated indoor environment free from corrosive gases or structural moisture.
⚠️ Clinical Precautions & Regulatory Disclaimer
- Professional Qualification Requirement: This product constitutes a high-risk Class III medical device kit. It must only be operated by qualified, certified orthopedic surgeons trained specifically in spinal fusion techniques within standardized clinical surgical environments.
- Preoperative Assessment: A comprehensive preoperative radiological assessment (CT/MRI/X-Ray) must be completed to thoroughly evaluate the patient's specific spinal anatomy and local bone mineral density.
- Contraindications: Absolutely contraindicated in cases involving acute systemic infections, localized infections at the intended surgical site, severe unmanaged osteoporosis, or advanced metabolic bone diseases with poor prognoses.
- Inspection Protocol: Prior to surgical incision, inspect the structural integrity of all instruments and verify that the sterilization indicator labels confirm successful processing. Do not use if any instrument shows signs of deformation, wear, or packaging damage.
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