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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MK femoral spacer distal ll/rm
implantcast GmbH
5722525000
In Commercial Distribution

  • 04048844589820 ()

  • sz. 2.5 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722520000
In Commercial Distribution

  • 04048844589813 ()

  • sz. 2 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722560500
In Commercial Distribution

  • 04048844589776 ()

  • sz. 6 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722550500
In Commercial Distribution

  • 04048844589769 ()

  • sz. 5 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722540500
In Commercial Distribution

  • 04048844589745 ()

  • sz. 4 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722530500
In Commercial Distribution

  • 04048844589738 ()

  • sz. 3 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722525500
In Commercial Distribution

  • 04048844589721 ()

  • sz. 2.5 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer distal ll/rm
implantcast GmbH
5722520500
In Commercial Distribution

  • 04048844589714 ()

  • sz. 2 / 5 mm


  • Knee arthroplasty wedge
Posterior Femoral Wedge - Thick - Size 7-8
MEDISURGE LLC
Posterior Thick 7-8
In Commercial Distribution

  • G611WZC26660 ()
WZ-C-2666

  • Knee arthroplasty wedge
Posterior Femoral Wedge - Thin - Size 7-8
MEDISURGE LLC
Posterior Thin 7-8
In Commercial Distribution

  • G611WZC26650 ()
WZ-C-2665

  • Knee arthroplasty wedge
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