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 posterior
implantcast GmbH
5722251000
In Commercial Distribution

  • 04048844589516 ()

  • sz. 2.5 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722201000
In Commercial Distribution

  • 04048844589509 ()

  • sz. 2 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722600500
In Commercial Distribution

  • 04048844589486 ()

  • sz. 6 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722500500
In Commercial Distribution

  • 04048844589479 ()

  • sz. 5 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722400500
In Commercial Distribution

  • 04048844589462 ()

  • sz. 4 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722300500
In Commercial Distribution

  • 04048844589455 ()

  • sz. 3 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722200500
In Commercial Distribution

  • 04048844589431 ()

  • sz. 2 / 5 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722250500
In Commercial Distribution

  • 04048844589448 ()

  • sz. 2.5 / 5 mm


  • Knee arthroplasty wedge
Hinge Femoral Distal Augment
Howmedica Osteonics Corp.
5612-D-605
In Commercial Distribution

  • 07613327555981 ()

  • Thickness: 5.0 Millimeter
  • Size: 6
5612-D-605

  • Knee arthroplasty wedge
Hinge Femoral Distal Augment
Howmedica Osteonics Corp.
5612-D-610
In Commercial Distribution

  • 07613327555974 ()

  • Size: 6
  • Thickness: 10.0 Millimeter
5612-D-610

  • Knee arthroplasty wedge
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