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Orthopedic product portfolio

CR Knee Systems

NMPA registeredRegistration scope available on request.

Cruciate-retaining femoral components, articular inserts, tibial components and patellar options.

Products

Showing 4 product families

CR Knee Systems

Primary PS and CR knee reconstruction

Tibial Component

CoCrMo tibial component for the compatible PS and CR Kirin primary knee systems.

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CR Knee Systems

Primary CR knee reconstruction

CR Femoral Component

Cruciate-retaining femoral component for the primary Kirin knee system, supplied in left and right configurations.

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CR knee systems

Build the CR knee configuration around compatibility.

Cruciate-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.

Confirm CR femoral sizing

Define the CR femoral component model, size and left or right configuration.

Match the CR insert and tibial platform

Confirm the CR articular insert size and thickness against the selected tibial component.

Review patellar and instrument options

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.

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Buyer FAQ

Questions to resolve before requesting a quote.

How do our products compare to top-tier international brands?

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.

What distinguishes a CR knee system from a PS system?

They use different femoral and articular insert designs intended for different procedural requirements. Confirm the approved configuration with the manufacturer and clinical team.

Can the tibial tray be shared between PS and CR systems?

Only where the manufacturer confirms compatibility. The insert, locking interface and instrument set should be reviewed as a complete system.

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