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 10mm, size 2
Medacta International SA
02.07.210FPW
In Commercial Distribution

  • 07630030820601 ()


  • Knee arthroplasty wedge
Femoral wedge distal 4mm, size 2
Medacta International SA
02.07.204FDW
In Commercial Distribution

  • 07630030820434 ()


  • Knee arthroplasty wedge
Femoral wedge distal 12mm, size 1
Medacta International SA
02.07.112FDW
In Commercial Distribution

  • 07630030819827 ()


  • Knee arthroplasty wedge
Femoral wedge posterior 10mm, size 1
Medacta International SA
02.07.110FPW
In Commercial Distribution

  • 07630030819810 ()


  • Knee arthroplasty wedge
Femoral wedge distal 4mm, size 1
Medacta International SA
02.07.104FDW
In Commercial Distribution

  • 07630030819674 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 6/10mm - Ti6Al4V
Medacta International SA
02.07.7610FPW
In Commercial Distribution

  • 07630040721752 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 4/5mm - Ti6Al4V
Medacta International SA
02.07.7405FPW
In Commercial Distribution

  • 07630040721608 ()


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

  • 07630040721486 ()


  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE FULL POROUS 46mm
DEPUY (IRELAND)
1294-53-246
In Commercial Distribution

  • 10603295026365 ()
129453246

  • Knee arthroplasty wedge
UNIVERSAL FEMORAL SLEEVE DISTAL POROUS 46mm
DEPUY (IRELAND)
1294-53-245
In Commercial Distribution

  • 10603295026358 ()
129453245

  • Knee arthroplasty wedge
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