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

Show Filters

PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S2 SMALL
Smith & Nephew, Inc.
71520023
Not in Commercial Distribution

  • 03596010227966 ()
71520023

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S1 LARGE
Smith & Nephew, Inc.
71520014
Not in Commercial Distribution

  • 03596010227935 ()
71520014

  • Knee arthroplasty wedge
PROFIX NONPOR DISTAL ONLY FEMORAL WEDGE S1 SMALL
Smith & Nephew, Inc.
71520013
Not in Commercial Distribution

  • 03596010227928 ()
71520013

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE5-6 10MM XSHRT
Smith & Nephew, Inc.
71420710
Not in Commercial Distribution

  • 03596010209047 ()
71420710

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE3-4 10MM XSHRT
Smith & Nephew, Inc.
71420708
Not in Commercial Distribution

  • 03596010209030 ()
71420708

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 7-8 5MMXSHORT
Smith & Nephew, Inc.
71420706
Not in Commercial Distribution

  • 03596010209023 ()
71420706

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 5-6 5MMXSHORT
Smith & Nephew, Inc.
71420704
Not in Commercial Distribution

  • 03596010209016 ()
71420704

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 3-4 5MMXSHORT
Smith & Nephew, Inc.
71420702
Not in Commercial Distribution

  • 03596010209009 ()
71420702

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE7-8 10MM SHORT
Smith & Nephew, Inc.
71420698
Not in Commercial Distribution

  • 03596010208989 ()
71420698

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE5-6 10MM SHORT
Smith & Nephew, Inc.
71420696
Not in Commercial Distribution

  • 03596010208972 ()
71420696

  • Knee arthroplasty wedge
< 1 ... 95 96 97 98 99 ... 143 >