The M6 posterior cervical spinal screw-rod system which is designed on the basis of the physiological characteristics of the human skeleton, is used for the internal fixation for the fracture. It consists of rod, crosslinks, laminar hook, lateral connector, occipital plate, occipital screw, occipital screws connector, domino connector, poly-axial thoracic screw, etc.
This M6 posterior cervical spinal screw-rod system is made through the mechanical processing and special surface treatment. The processing materials for the spinal internal fixation system are the GB/T13810 specified titanium and titanium alloy. Moreover, our product is in compliance with the registered product standard of the Spinal Internal Fixation System.
Service Life
Prior to the fracture healing, the internal fixation instrument is the main role to withstand the physiological load. Commonly, the implant should be removed after approximately one year's healing. Otherwise, the potential risk of secondary fracture and implant breakage will exist. Please follow your doctor's advice, and timely contact your doctor if you are feeling unwell. After the fracture healing, it is normal that the implant has breakage resulted from the not timely removal.
Product No. | Diameter (mm) | Length(mm) |
11141-(006 ~ 024) | 3.5 | 10 ~ 24 |
11141-(110 ~ 152) | 4 | 10 ~ 52 |
Note: In 2.0mm increments
Product No. | Width of Hook(mm) |
11142-045 | 4.5 |
11142-060 | 6 |
Product No. | Diameter (mm) | Length(mm) |
11144-120 | 3.2 | 120 |
11144-240 | 240 |
Product No. | Length(mm) |
11145 | 10 |
Product No. | Length(mm) |
11146 | 40/45/50 |
Product No. | Width (mm) |
11147-(024/032/040) | 24/32/40 |
Product No. | Diameter (mm) | Length(mm) |
11148-(010 ~ 032) | HB3.5 | 10 ~ 32 |
11148-(110 ~ 132) | HB4.0 | 10 ~ 32 |
Note: In 2.0mm increments
Product No. | Diameter(mm) |
11149-032 | 3.2 |
Product No. | Diameter(mm) |
11150-(045/055) | 4.5/5.5 |
Material: Titanium Alloy
Package: One piece per package
Package and Sterilization Treatment
The product is supplied in the non-sterile package. After originally packed with the paper plastic package, the product will be put into the plastic bag together with the Operation Instructions and the Product Qualification Certificates.
The paper plastic roll bag is used as the inner package. It is compounded from the medical dialysis paper and plastic film. The production environment is controlled with the cleanness of Class 10,000. In the cleaning shop, the package bag is cut according to the product size. Then, its one side will be sealed with the heat-sealing machine. After the bag has been used to contain the product, its other side needs to be sealed with the sealing machine.
The paper plastic, into which the product has been put, will be cleaned in the controlling area where the cleanliness is of Class 10,000. All the cleaning methods have been inspected. The product packed with this method needs no cleaning prior to use. It just needs to be treated with sterilization in accordance with the methods specified in the Product Instructions.
Related Names
Spine Surgery Instrument | Cervical Spine Implants | Cervical Screws