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ODM Spine Titanium Minimally Invasive Pedicle Screws Manufacturer, Pricelist
Product Description
📋 Specifications & System Matrix
| Component | Specification / Size |
|---|---|
Zenith SE Mono-Angle Screw
|
Φ5.5 x 35 mm |
| Φ5.5 x 40 mm | |
| Φ6.0 x 40 mm | |
| Φ6.0 x 45 mm | |
| Φ6.5 x 40 mm | |
| Φ6.5 x 45 mm | |
| Φ6.5 x 50 mm | |
Zenith SE Multi-Angle Screw
|
Φ5.5 x 35 mm |
| Φ5.5 x 40 mm | |
| Φ6.0 x 40 mm | |
| Φ6.0 x 45 mm | |
| Φ6.5 x 35 mm | |
| Φ6.5 x 40 mm | |
| Φ6.5 x 45 mm | |
| Φ6.5 x 50 mm | |
Zenith SE Breakable Set Screw
|
N/A |
MIS Connection Rod (Straight)
|
Φ5.5 x 40 mm |
| Φ5.5 x 45 mm | |
| Φ5.5 x 50 mm | |
| Φ5.5 x 55 mm | |
| Φ5.5 x 60 mm | |
| Φ5.5 x 65 mm | |
| Φ5.5 x 70 mm | |
| Φ5.5 x 75 mm | |
| Φ5.5 x 80 mm | |
| Φ5.5 x 85 mm | |
| Φ5.5 x 90 mm | |
| Φ5.5 x 95 mm | |
| Φ5.5 x 100 mm | |
| Φ5.5 x 105 mm | |
| Φ5.5 x 110 mm | |
| Φ5.5 x 115 mm | |
| Φ5.5 x 120 mm | |
| Φ5.5 x 125 mm | |
| Φ5.5 x 130 mm | |
| Φ5.5 x 135 mm | |
| Φ5.5 x 140 mm | |
| Φ5.5 x 145 mm | |
| Φ5.5 x 150 mm | |
| Φ5.5 x 155 mm | |
| Φ5.5 x 160 mm | |
| Φ5.5 x 165 mm | |
| Φ5.5 x 170 mm | |
| Φ5.5 x 180 mm | |
| Φ5.5 x 190 mm | |
| Φ5.5 x 200 mm | |
MIS Connection Rod (Pre-Bent)
|
Φ5.5 x 40 mm |
| Φ5.5 x 45 mm | |
| Φ5.5 x 50 mm | |
| Φ5.5 x 55 mm | |
| Φ5.5 x 60 mm | |
| Φ5.5 x 65 mm | |
| Φ5.5 x 70 mm | |
| Φ5.5 x 75 mm | |
| Φ5.5 x 80 mm | |
| Φ5.5 x 85 mm | |
| Φ5.5 x 90 mm | |
| Φ5.5 x 95 mm | |
| Φ5.5 x 100 mm | |
| Φ5.5 x 105 mm | |
| Φ5.5 x 110 mm | |
| Φ5.5 x 115 mm | |
| Φ5.5 x 120 mm | |
| Φ5.5 x 125 mm | |
| Φ5.5 x 130 mm | |
| Φ5.5 x 135 mm | |
| Φ5.5 x 140 mm | |
| Material | Titanium Alloy |
| Surface Treatment | Micro-arc Oxidation |
| Qualification | CE/ISO13485/NMPA |
| Package | Sterile Packaging 1pcs/package |
| MOQ | 1 Pcs |
| Supply Ability | 1000+Pieces per Month |
⚙️ Key Structural Features & Advantages
✓
The low profile better counters the anterior margin of the posterior column for reducing the risk of intraoperative screw breaking. The thread design for cortical and cancellous bone can meet patients with various bone quality.
✓
The unique design of soft extension improves the intraoperative operability. The soft tabs avoid the intraoperative mutual interference in the operation. The intraoperatively visible and touchable facilitates multilevel rod-passing. The whole passing process doesn't need the auxiliary positioning with X-ray.
🎯 Clinical Indications
★
Provide posterior, noncervical fixation as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e., fracture or dislocation); spinal stenosis; curvatures (i.e., scoliosis, kyphosis and/or lordosis); tumor; pseudarthritis; and/or failed previous fusion.
⚖️ Soft Extension VS Hard Extension
Soft Extension VS Hard Extension
1. During the multilevel or lower lumbar cases, the hard tabs intersect each other and may break.
2. The muscular counterforce gets the hard tabs closer, which interferes intraoperative observation.
3. The hard tabs require high precision of instruments for rod passing and X-ray assist. These delay the time and increase damage to surgeons.
1. During the multilevel or lower lumbar cases, the hard tabs intersect each other and may break.
2. The muscular counterforce gets the hard tabs closer, which interferes intraoperative observation.
3. The hard tabs require high precision of instruments for rod passing and X-ray assist. These delay the time and increase damage to surgeons.
🔒 Reliable Design & Safety
More Reliable Design
Unique locking from both lateral and medial integrates the soft tab and screw together firmly, avoiding the tab detaching during rod passing and pressing.
Soft tab and screw only connected laterally may detach during rod passing and pressing and delay operating time. The screw cannot be close to anterior margin of the posterior column. The remained profile will make intraoperative tab breaking difficult and lead postoperative screw breaking.
Unique locking from both lateral and medial integrates the soft tab and screw together firmly, avoiding the tab detaching during rod passing and pressing.
Soft tab and screw only connected laterally may detach during rod passing and pressing and delay operating time. The screw cannot be close to anterior margin of the posterior column. The remained profile will make intraoperative tab breaking difficult and lead postoperative screw breaking.
Breakable Setscrew
ZATH’s
Others’
The low profile better counters the anterior margin of the posterior column for reducing the risk of intraoperative screw breaking. The thread design for cortical and cancellous bone can meet patients with various bone quality.
Arcuate Rod Geometry
1. Decrease intraoperative rod bending and reduce breaking rate.
2. Unique design of rod holding for easy operation
1. Decrease intraoperative rod bending and reduce breaking rate.
2. Unique design of rod holding for easy operation
12.5 N.M intraoperative locking Easy operation
❓ Frequently Asked Questions (FAQ)
Q1: What material is used for the Zenith SE Spinal System?
The implants are precision manufactured from medical-grade Titanium Alloy with Micro-arc Oxidation surface treatment, offering optimal biocompatibility and high mechanical endurance.
Q2: What are the advantages of soft extension tabs over rigid hard tabs?
Soft extension tabs prevent intraoperative tab intersection and fracture during multilevel surgeries. They minimize interference from muscular counterforce and allow for rod-passing without mandatory X-ray auxiliary guidance.
Q3: What is the recommended intraoperative locking torque?
The recommended intraoperative locking torque is 12.5 N·m, ensuring rigid and stable fixation with easy instrumentation handling.
Q4: How does the thread design adapt to different bone types?
The pedicle screws feature specialized dual-thread designs suitable for both cortical and cancellous bone, providing strong purchase across varying patient bone qualities.
Q5: What clinical indications is this system approved for?
It is indicated for noncervical posterior fixation in treating degenerative disc disease, spondylolisthesis, spinal trauma, spinal stenosis, spinal curvatures (scoliosis, kyphosis, lordosis), tumors, pseudarthrosis, and revision surgeries.
Q6: What regulatory certifications do these orthopedic implants hold?
The components are fully certified under international quality standards including CE, ISO13485, and NMPA qualifications, packaged in sterile single-unit blisters.
