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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Femoral Posterior Augmentation # 6/4mm - Ti6Al4V
Medacta International SA
02.07.7604FPW
In Commercial Distribution

  • 07630971258396 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 5/8mm - Ti6Al4V
Medacta International SA
02.07.7508FPW
In Commercial Distribution

  • 07630971258389 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 5/4mm - Ti6Al4V
Medacta International SA
02.07.7504FPW
In Commercial Distribution

  • 07630971258372 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 4/8mm - Ti6Al4V
Medacta International SA
02.07.7408FPW
In Commercial Distribution

  • 07630971258365 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 4/4mm - Ti6Al4V
Medacta International SA
02.07.7404FPW
In Commercial Distribution

  • 07630971258358 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 3/8mm - Ti6Al4V
Medacta International SA
02.07.7308FPW
In Commercial Distribution

  • 07630971258341 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 3/4mm - Ti6Al4V
Medacta International SA
02.07.7304FPW
In Commercial Distribution

  • 07630971258334 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 2/8mm - Ti6Al4V
Medacta International SA
02.07.7208FPW
In Commercial Distribution

  • 07630971258327 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 2/4mm - Ti6Al4V
Medacta International SA
02.07.7204FPW
In Commercial Distribution

  • 07630971258310 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 1/8mm - Ti6Al4V
Medacta International SA
02.07.7108FPW
In Commercial Distribution

  • 07630971258303 ()


  • Knee arthroplasty wedge
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