Primary PS and CR knee reconstruction
Tibial Component
CoCrMo tibial component for the compatible PS and CR Kirin primary knee systems.
View product →Cruciate-retaining femoral components, articular inserts, tibial components and patellar options.
Primary PS and CR knee reconstruction
CoCrMo tibial component for the compatible PS and CR Kirin primary knee systems.
View product →Patellar reconstruction
UHMWPE patellar component with four diameter options for compatible primary knee reconstruction.
View product →Primary CR knee reconstruction
Cruciate-retaining femoral component for the primary Kirin knee system, supplied in left and right configurations.
View product →Primary CR knee reconstruction
Cruciate-retaining UHMWPE tibial articular insert supplied across multiple sizes and insert thicknesses.
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Ask our product teamCruciate-retaining knee systems use a distinct femoral component and CR articular insert with compatible tibial and instrument options. Confirm the complete configuration before requesting a quotation.
Define the CR femoral component model, size and left or right configuration.
Confirm the CR articular insert size and thickness against the selected tibial component.
Clarify whether patellar resurfacing is required and confirm the corresponding instrumentation and supply scope.
CR and PS components are not interchangeable without manufacturer confirmation. Final selection remains with qualified clinicians.
Discuss your requirements →Our hip and knee systems are independently engineered with reference to established J&J product configurations. The default size range is aligned with Southeast Asian anatomical proportions, with larger implant options available for European and North American requirements. Gather is not affiliated with or endorsed by Johnson & Johnson; final sizing, compatibility and market documentation must be confirmed against the approved product information.
They use different femoral and articular insert designs intended for different procedural requirements. Confirm the approved configuration with the manufacturer and clinical team.
Only where the manufacturer confirms compatibility. The insert, locking interface and instrument set should be reviewed as a complete system.