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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GEN II POSTERIOR FEMORAL WEDGE SIZE 7-8 5MM SHORT
Smith & Nephew, Inc.
71420692
Not in Commercial Distribution

  • 03596010208958 ()
71420692

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 5-6 5MM SHORT
Smith & Nephew, Inc.
71420690
Not in Commercial Distribution

  • 03596010208941 ()
71420690

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE 1-2 5MM SHORT
Smith & Nephew, Inc.
71420686
Not in Commercial Distribution

  • 03596010208927 ()
71420686

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 8 RIGHT
Smith & Nephew, Inc.
71420062
In Commercial Distribution

  • 03596010205742 ()
71420062

  • Knee arthroplasty wedge
GENESIS II C/R POROUS FEMORAL SIZE 7 RIGHT
Smith & Nephew, Inc.
71420060
In Commercial Distribution

  • 03596010205735 ()
71420060

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 6 RIGHT
Smith & Nephew, Inc.
71420058
In Commercial Distribution

  • 03596010205728 ()
71420058

  • Knee arthroplasty wedge
GENESIS II C/R POROUS FEMORAL SIZE 5 RIGHT
Smith & Nephew, Inc.
71420056
In Commercial Distribution

  • 03596010205711 ()
71420056

  • Knee arthroplasty wedge
GENESIS II C/R POROUS FEMORAL SIZE 4 RIGHT
Smith & Nephew, Inc.
71420054
In Commercial Distribution

  • 03596010205704 ()
71420054

  • Knee arthroplasty wedge
GENESIS II C/R POROUS FEMORAL SIZE 3 RIGHT
Smith & Nephew, Inc.
71420052
In Commercial Distribution

  • 03596010205698 ()
71420052

  • Knee arthroplasty wedge
GENESIS II CRUCIATE RETAINING POROUS FEMORAL SIZE 2 RIGHT
Smith & Nephew, Inc.
71420050
In Commercial Distribution

  • 03596010205681 ()
71420050

  • Knee arthroplasty wedge
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