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 # 3/10mm - Ti6Al4V
Medacta International SA
02.07.7310FPW
In Commercial Distribution

  • 07630040721554 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 1/5mm - Ti6Al4V
Medacta International SA
02.07.7105FPW
In Commercial Distribution

  • 07630040721394 ()


  • 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
Femoral Augmentation distal # 5/16 mm
Medacta International SA
02.07.516FDA
In Commercial Distribution

  • 07630030888946 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 4/20 mm
Medacta International SA
02.07.420FDA
In Commercial Distribution

  • 07630030888939 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 4/16 mm
Medacta International SA
02.07.416FDA
In Commercial Distribution

  • 07630030888922 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 3/20 mm
Medacta International SA
02.07.320FDA
In Commercial Distribution

  • 07630030888915 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 3/16 mm
Medacta International SA
02.07.316FDA
In Commercial Distribution

  • 07630030888908 ()


  • Knee arthroplasty wedge
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