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 POST/STAB FEMORAL WEDGE SPACER SZ4 SMALL
Smith & Nephew, Inc.
71512484
In Commercial Distribution

  • 23596010224167 ()
  • 03596010224163 ()
71512484

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ3 LARGE
Smith & Nephew, Inc.
71512483
In Commercial Distribution

  • 23596010224150 ()
  • 03596010224156 ()
71512483

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ3 SMALL
Smith & Nephew, Inc.
71512482
In Commercial Distribution

  • 23596010224143 ()
  • 03596010224149 ()
71512482

  • Knee arthroplasty wedge
PROFIX POST/STAB FEMORAL WEDGE SPACER SZ2 LARGE
Smith & Nephew, Inc.
71512481
In Commercial Distribution

  • 23596010224136 ()
  • 03596010224132 ()
71512481

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S7 LARGE
Smith & Nephew, Inc.
71500074
Not in Commercial Distribution

  • 03596010218292 ()
71500074

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLYF FEMORAL WEDGE S6 SMALL
Smith & Nephew, Inc.
71500063
Not in Commercial Distribution

  • 03596010218247 ()
71500063

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S4 LARGE
Smith & Nephew, Inc.
71500044
Not in Commercial Distribution

  • 03596010218179 ()
71500044

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S4 SMALL
Smith & Nephew, Inc.
71500043
Not in Commercial Distribution

  • 03596010218162 ()
71500043

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S3 LARGE
Smith & Nephew, Inc.
71500034
Not in Commercial Distribution

  • 03596010218131 ()
71500034

  • Knee arthroplasty wedge
PROFIX POROUS DISTAL ONLY FEMORAL WEDGE S3 SMALL
Smith & Nephew, Inc.
71500033
Not in Commercial Distribution

  • 03596010218124 ()
71500033

  • Knee arthroplasty wedge
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