Miss Spinal System II, Pedicle Screws and Universal Pedicle Screws

Product Details
Customization: Available
Customized: Non-Customized
Certification: ISO, CE
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  • Miss Spinal System II, Pedicle Screws and Universal Pedicle Screws
  • Miss Spinal System II, Pedicle Screws and Universal Pedicle Screws
  • Miss Spinal System II, Pedicle Screws and Universal Pedicle Screws
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  • Overview
  • Product Description
  • Indications
  • Contraindications
  • Product Parameters
  • Our Advantages
  • Instrument set
  • Inside Our Company
Overview

Basic Info.

Model NO.
Diameter 5.0/ 5.5/ 6.0/ 6.5/ 7.0mm
Condition
New
Usage
Correct Deformities, Fracture Fixation
Using Site
Vertebra, Spinal Pedicle
Type
Spinal Internal Fixation
Product Code
9901
Diameter
5.0/ 5.5/ 6.0/ 6.5/ 7.0mm
Indications
Degenerative Lumbar Disorders, Spinal Fractures
Material Type Details
Medical-Grade Titanium for Biocompatibility
Sterility
Non-Sterile, Requires Sterilization Before Use
Reusable or Single-Use
Single-Use Implant
Contraindications
Active Infection, Allergic Reactions
Transport Package
1 PC/Package
Specification
Medical grade Titanium
Trademark
BEST MEDICAL
Origin
China
HS Code
9021100000
Production Capacity
500000 PCS/Year

Product Description

Product Description

MISS Pedicle Screw II Features:

  • Made from high-quality titanium for superior strength, biocompatibility, and corrosion resistance.
  • Specifically designed for advanced minimally invasive spinal surgery (MISS) with the capability to inject bone cement for enhanced fixation.
  • Bone cement augmentation allows for increased stabilization in osteoporotic or compromised bone, providing better fixation in spinal fusion procedures.
  • Available in various diameters and lengths, ensuring versatility to meet different spinal stabilization needs.
  • Suitable for thoracic and lumbar spine surgeries, especially for patients with weakened bone structure where bone cement can improve screw fixation.
MISS Universal Pedicle Screw II Features:
  • Titanium construction ensures strength and biocompatibility, along with the ability to inject bone cement for enhanced fixation in complex spinal stabilization cases.
  • Bone cement injection improves anchoring in the vertebrae, especially in osteoporotic bones or in cases where additional stabilization is required.
  • Available in multiple diameters and lengths to meet different patient anatomies and fracture patterns, making it ideal for both lumbar and thoracic spine procedures.
  • Provides excellent stabilization with the ability to inject bone cement directly into the vertebral body, improving the fixation strength in minimally invasive spinal procedures.
 
 
Indications

Indications:

  • Degenerative Lumbar Disorders: Indicated for spinal decompression and stabilization in cases of lumbar disc herniation, degenerative disc disease, and spinal stenosis.
  • Spinal Fractures: Used for fixation of unstable thoracolumbar fractures, particularly osteoporotic fractures requiring cement augmentation.
  • Spinal Tumors: Suitable for stability reconstruction following spinal tumor resection, especially in cases where cement augmentation is needed in fragile bone structures.
  • Spinal Deformity Correction: Indicated for correction and fixation in spinal deformities such as scoliosis and kyphotic deformities.
  • Infectious Spinal Disorders: Provides stability support following debridement of infectious spinal conditions, such as spinal tuberculosis or other infectious lesions.

Contraindications

Contraindications:

  • Active Infection: Including local infection at the surgical site or systemic infection.
  • Severe Osteoporosis: While cement augmentation may provide reinforcement, extreme bone fragility may still result in implant failure.
  • Unhealed Fractures: Not recommended in cases where stable bone support cannot be provided.
  • Allergic Reactions: Patients with allergies to implant materials (e.g., titanium alloy) or cement components (e.g., polymethylmethacrylate, PMMA).
  • Severe Systemic Diseases: Patients who cannot tolerate anesthesia or surgery.
  • Unrelieved Spinal Cord Compression: Direct fixation is not advised in cases where spinal cord compression symptoms have not been appropriately managed.

Product Parameters

Specifications:


MISS Pedicle Screw II
Diameter (mm) Length (mm)
5.0 30, 35, 40, 45
5.5 35, 40, 45, 50
6.0 35, 40, 45, 50
6.5 35, 40, 45, 50
7.0 35, 40, 45, 50


MISS Universal Pedicle Screw II
Diameter (mm) Length (mm)
5.0 30, 35, 40
5.5 35, 40, 45
6.0 35, 40, 45, 50
6.5 35, 40, 45, 50
7.0 35, 40, 45, 50
 
Our Advantages

Bone Cement Augmentation Feature:
  • The key distinguishing feature of MISS Spinal System II is the ability to inject bone cement into the vertebral body through the pedicle screw during spinal fixation.
  • Bone cement augmentation enhances the stability of the screw, especially in osteoporotic patients or those with compromised bone quality.
  • This feature provides additional anchoring and reduces the risk of screw loosening or pullout, improving overall surgical outcomes in spinal fusion procedures.
 
Instrument set

Instrument Set:
The product is compatible with the instrument set for MISS pedicle screw II and MISS universal pedicle screw II, 9301-000.
 
Inside Our Company

Miss Spinal System II, Pedicle Screws and Universal Pedicle ScrewsMiss Spinal System II, Pedicle Screws and Universal Pedicle ScrewsMiss Spinal System II, Pedicle Screws and Universal Pedicle ScrewsMiss Spinal System II, Pedicle Screws and Universal Pedicle ScrewsMiss Spinal System II, Pedicle Screws and Universal Pedicle ScrewsMiss Spinal System II, Pedicle Screws and Universal Pedicle Screws

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