| Material | Polymer type | PEEK (polyether ether ketone); implant-grade formulations are available. | Confirm the material grade and applicable regulatory documentation for the intended medical use. |
| Material property | Tensile strength | Unfilled PEEK commonly has tensile strength in the approximate range of 90–100 MPa, depending on grade and test method. | Useful for material comparison; it does not by itself establish the strength of a finished screw. |
| Material property | Tensile modulus | Typically approximately 3.6–4.0 GPa for unfilled PEEK, with variation by grade and test conditions. | Provides context for stiffness. Finished-device performance also depends on screw geometry and loading. |
| Material property | Density | Approximately 1.30–1.32 g/cm³ for unfilled PEEK. | A relatively low-density material can support lightweight implant designs. |
| Material property | Thermal characteristics | Typical glass-transition temperature is about 143°C; melting temperature is about 343°C. | Processing and sterilization compatibility must be assessed for the specific material and validated device. |
| Imaging | Radiographic appearance | Unfilled PEEK is radiolucent compared with many metallic implant materials. | May allow clearer visualization of surrounding anatomy, although imaging results depend on the full device and imaging method. |
| Screw design | Thread profile and pitch | Thread form, pitch, depth, and cutting features are selected for the intended bone tunnel and surgical technique. | Check compatibility with the procedure, graft type, bone quality, and the specified insertion method. |
| Screw design | Tip geometry | Common design options include a tapered or rounded leading tip, with or without a self-tapping feature. | Tip design can affect initial positioning and insertion; follow the device instructions for use. |
| Screw design | Drive interface | Drive features are designed to engage a matching surgical driver and transmit insertion torque. | Verify driver compatibility and the manufacturer’s handling instructions to reduce the risk of interface damage. |
| Size selection | Diameter and length | Available sizes vary by device system and intended anatomical application. | Select dimensions according to the surgical plan, graft, tunnel, and device labeling rather than using a universal size. |
| Quality and compliance | Verification and documentation | Review material traceability, dimensional inspection, mechanical test data, sterilization information, and applicable market approvals. | Requirements differ by destination market and intended use; request current, device-specific documentation. |