Ti Posterior Thoracolumbar Rod-Screw System(6.0)
The Titanium Alloy Posterior Thoracolumbar Spinal System (6.0) is a posterior spinal fixation system designed for use in thoracic and lumbar spinal fixation procedures, subject to the product's approved indications for use. The system integrates compatible pedicle screws, connecting rods, locking components, and selected auxiliary components to support the assembly of a posterior spinal fixation construct.
For hospitals, orthopedic implant distributors, medical device importers, and surgical instrument procurement teams, selecting a spinal fixation system requires more than checking the product name. Component compatibility, screw configurations, dimensional specifications, material documentation, and the availability of matching surgical instruments should all be reviewed before procurement.
Explore the orthopedic implants and instruments range to compare related spinal fixation solutions, or contact ATOM to discuss product specifications and procurement requirements.
A posterior thoracolumbar pedicle screw and rod system consists of coordinated fixation components. The final configuration depends on the selected implant options, the approved product instructions, and the requirements of the treating surgical team.
Pedicle screws provide the primary vertebral anchoring points within a compatible posterior fixation construct. Different screw designs may be available to accommodate different fixation and reduction requirements.
Monoaxial pedicle screws for applications requiring a fixed screw-head orientation.
Polyaxial reduction screws for compatible constructs requiring angular flexibility and reduction features.
Additional screw configurations may be selected according to the available product models and approved system compatibility.
Connecting rods link the implanted screws to form the posterior fixation construct. Rod selection should account for the system diameter, available rod lengths, contouring requirements, and compatibility with the selected screw heads and locking components.
Buyers should confirm the available rod specifications and compatible locking components against the current product catalog rather than assuming that components from different systems can be interchanged.
Locking components secure the rod within compatible screw-head assemblies. Depending on the system configuration, different locking designs may be offered for specific procedural requirements.
View the self-breaking set screw for the 6.0 system for product-specific information.
Reduction components and auxiliary connectors may support selected construct configurations. Their availability and compatibility should be verified for the intended system and procedure.
For spinal deformity applications, review the Ti Posterior Rod-Screw for Spinal Deformity (6.0 System) and confirm the applicable indications and compatible components.
When sourcing a titanium alloy posterior thoracolumbar spinal system, procurement teams should evaluate the specifications of individual components as well as the compatibility of the assembled system. The following table identifies the key information to confirm with the manufacturer.
| Specification | Information to Confirm | Procurement Consideration |
|---|---|---|
| System designation | Posterior Thoracolumbar Spinal System (6.0) | Confirm the exact system version and product codes. |
| Implant material | Confirm the material for each selected component. | Request the applicable material specifications and documentation. |
| Screw types | Monoaxial, polyaxial, reduction, and other available designs | Verify availability, dimensions, and system compatibility. |
| Screw dimensions | Available diameters and lengths for each model | Confirm the required sizes using the current product catalog. |
| Connecting rods | Compatible diameter, length, and available configurations | Check compatibility with the selected screw and locking components. |
| Locking components | Available set screw and locking designs | Confirm compatibility with the selected implant configuration. |
| Surgical instruments | Compatible instrument set and required accessories | Confirm whether instruments are included or supplied separately. |
| Packaging and documentation | Packaging configuration, labeling, instructions for use, and applicable certificates | Verify the requirements of the destination market and purchasing institution. |
Specific dimensions, available models, material grades, packaging configurations, and regulatory documentation should be confirmed with ATOM before placing an order.
Posterior thoracolumbar spinal fixation systems are used in surgical procedures involving stabilization of selected spinal segments. The applicable indications depend on the specific device, its approved labeling, and the clinical assessment of the treating surgeon.
Posterior screw-and-rod constructs may be used to stabilize selected thoracic and lumbar spinal segments when indicated. The required fixation configuration depends on the anatomical level, the treatment plan, and the compatible implant options.
For eligible deformity correction procedures, compatible fixation components may be configured to support the planned correction and stabilization. Review the relevant system options and confirm their approved indications before selection.
Certain posterior fixation systems are indicated for selected spinal fractures and instability conditions. Buyers should verify the intended use of this specific system rather than relying on indications published for other manufacturers' products.
Begin by identifying the intended system, the required component types, and the relevant product models. A clear component list helps purchasing teams avoid ordering incompatible screws, rods, or locking parts.
Confirm the available screw diameters and lengths, rod dimensions, and compatible locking components using the manufacturer's current specifications. The 6.0 system designation should not be interpreted as a guarantee that every component has the same diameter.
Request the material specifications, instructions for use, product identification information, and applicable regulatory documentation required for the destination market. Do not assume that a certification or approval for another product automatically applies to this system.
Implant selection and instrument selection should be evaluated together. Review the 6.0 Posterior Thoracolumbar Spinal System Instrument Set and confirm the compatible instruments, accessories, and ordering scope with the manufacturer.
For medical device distributors, hospital procurement teams, and orthopedic implant suppliers, a reliable sourcing process depends on accurate product identification, clear specifications, and consistent communication with the manufacturer.
ATOM provides a range of orthopedic implants and instruments. Buyers can review related spinal fixation products to identify the appropriate product family for their requirements.
Compare the Ti Posterior Thoracolumbar Rod-Screw System (5.5) with the 6.0 system when evaluating alternative system configurations. The two systems should be assessed according to their individual specifications and compatibility requirements.
Before ordering, request the current product catalog, model numbers, available dimensions, component compatibility information, applicable quality documentation, and supply details. This information helps procurement teams evaluate product suitability and prepare accurate purchasing specifications.
It is an implant system used in selected surgical procedures to stabilize spinal segments through a posterior approach. Depending on the system, its components may include pedicle screws, connecting rods, locking components, and auxiliary connectors.
The designation identifies the system's specified size category. Buyers should consult the manufacturer's documentation to confirm the dimensions of individual components and their compatibility.
The system is presented as a titanium alloy posterior thoracolumbar spinal system. Confirm the exact alloy grade and applicable material standards for each component using the current product documentation.
ATOM lists different screw configurations within its 6.0 product family, including monoaxial and reduction screw options. Contact the manufacturer to confirm the current model range, dimensions, and compatibility requirements.
The ordering scope should be confirmed with the manufacturer. Ask whether the required instruments are supplied separately, which instrument set is compatible with the selected implants, and which components are included in the quotation.
Provide the required system version, component types, model numbers or dimensions, estimated quantities, destination market, documentation requirements, and any instrument-set requirements. If the exact configuration is not yet finalized, request the current catalog and compatibility information first.
Looking for a posterior thoracolumbar spinal fixation system for your orthopedic implant portfolio or procurement requirements? Contact ATOM to request the current product catalog, available component specifications, compatible instrument information, and a quotation based on your requirements.
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