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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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GMK Sphere Revision Posterior Wedge S2 12mm
Medacta International SA
02.19.PA12
In Commercial Distribution

  • 07630345718921 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S2 8mm
Medacta International SA
02.19.PA08
In Commercial Distribution

  • 07630345718914 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S2 4mm
Medacta International SA
02.19.PA04
In Commercial Distribution

  • 07630345718907 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S7/8 20mm
Medacta International SA
02.19.DD20
In Commercial Distribution

  • 07630345718891 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S7/8 16mm
Medacta International SA
02.19.DD16
In Commercial Distribution

  • 07630345718884 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S7/8 12mm
Medacta International SA
02.19.DD12
In Commercial Distribution

  • 07630345718877 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S7/8 8mm
Medacta International SA
02.19.DD08
In Commercial Distribution

  • 07630345718860 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S7/8 4mm
Medacta International SA
02.19.DD04
In Commercial Distribution

  • 07630345718853 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S5/6 20mm
Medacta International SA
02.19.DC20
In Commercial Distribution

  • 07630345718846 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Distal Wedge S5/6 16mm
Medacta International SA
02.19.DC16
In Commercial Distribution

  • 07630345718839 ()


  • Knee arthroplasty wedge
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