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 wedge posterior 5mm, size 1
Medacta International SA
02.05.01PW
In Commercial Distribution

  • 07630030814778 ()


  • Knee arthroplasty wedge
Femoral wedge distal 8mm, size 1
Medacta International SA
02.05.01DW
In Commercial Distribution

  • 07630030814761 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 5/5mm - Ti6Al4V
Medacta International SA
02.07.7505FPW
In Commercial Distribution

  • 07630040721677 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 4/10mm - Ti6Al4V
Medacta International SA
02.07.7410FPW
In Commercial Distribution

  • 07630040721622 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 3/5mm - Ti6Al4V
Medacta International SA
02.07.7305FPW
In Commercial Distribution

  • 07630040721530 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 2/10mm - Ti6Al4V
Medacta International SA
02.07.7210FPW
In Commercial Distribution

  • 07630040721486 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 1/10mm - Ti6Al4V
Medacta International SA
02.07.7110FPW
In Commercial Distribution

  • 07630040721417 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 6/20 mm
Medacta International SA
02.07.620FDA
In Commercial Distribution

  • 07630030888977 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 6/16 mm
Medacta International SA
02.07.616FDA
In Commercial Distribution

  • 07630030888960 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 5/20 mm
Medacta International SA
02.07.520FDA
In Commercial Distribution

  • 07630030888953 ()


  • Knee arthroplasty wedge
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