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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GENESIS II DISTAL FEMORAL WEDGE SIZE 4 5MM
Smith & Nephew, Inc.
71420667
Not in Commercial Distribution

  • 03596010208774 ()
71420667

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE SIZE 3 5MM
Smith & Nephew, Inc.
71420666
Not in Commercial Distribution

  • 03596010208767 ()
71420666

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE SIZE 2 5MM
Smith & Nephew, Inc.
71420665
Not in Commercial Distribution

  • 03596010208750 ()
71420665

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE SIZE 1 5MM
Smith & Nephew, Inc.
71420664
Not in Commercial Distribution

  • 03596010208743 ()
71420664

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE SZ7 FULL
Smith & Nephew, Inc.
71520074
Not in Commercial Distribution

  • 03596010228178 ()
71520074

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S7 LARGE
Smith & Nephew, Inc.
71520073
Not in Commercial Distribution

  • 03596010228161 ()
71520073

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S6 LARGE
Smith & Nephew, Inc.
71520064
Not in Commercial Distribution

  • 03596010228130 ()
71520064

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S6 SMALL
Smith & Nephew, Inc.
71520063
Not in Commercial Distribution

  • 03596010228123 ()
71520063

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S5 LARGE
Smith & Nephew, Inc.
71520054
Not in Commercial Distribution

  • 03596010228093 ()
71520054

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S4 LARGE
Smith & Nephew, Inc.
71520044
Not in Commercial Distribution

  • 03596010228055 ()
71520044

  • Knee arthroplasty wedge
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