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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PROFIX FEMORAL WEDGE SIZE 2 LARGE
Smith & Nephew, Inc.
71500022
Not in Commercial Distribution

  • 03596010218070 ()
71500022

  • Knee arthroplasty wedge
3DMetal Diaphyseal Femoral Cone Size Small
Medacta International SA
02.07.FCS20
In Commercial Distribution

  • 07630971259232 ()


  • Knee arthroplasty wedge
3DMetal Diaphyseal Femoral Cone Size Medium
Medacta International SA
02.07.FCM25
In Commercial Distribution

  • 07630971259225 ()


  • Knee arthroplasty wedge
3DMetal Diaphyseal Femoral Cone Size Large
Medacta International SA
02.07.FCL30
In Commercial Distribution

  • 07630971259218 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 6/8mm - Ti6Al4V
Medacta International SA
02.07.7608FPW
In Commercial Distribution

  • 07630971258402 ()


  • Knee arthroplasty wedge
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
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