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 NON POROUS C/R FEMORAL SIZE 5 RIGHT
Smith & Nephew, Inc.
71420024
In Commercial Distribution

  • 03596010205551 ()
71420024

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 4 RIGHT
Smith & Nephew, Inc.
71420022
In Commercial Distribution

  • 03596010205544 ()
71420022

  • Knee arthroplasty wedge
GENESIS II NON POROUS C/R FEMORAL SIZE 3 RIGHT
Smith & Nephew, Inc.
71420020
In Commercial Distribution

  • 03596010205537 ()
71420020

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 2 RIGHT
Smith & Nephew, Inc.
71420018
In Commercial Distribution

  • 03596010205520 ()
71420018

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 1 RIGHT
Smith & Nephew, Inc.
71420016
In Commercial Distribution

  • 03596010205513 ()
71420016

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 8 LEFT
Smith & Nephew, Inc.
71420014
In Commercial Distribution

  • 03596010205506 ()
71420014

  • Knee arthroplasty wedge
GENESIS II NON POROUS C/R FEMORAL SIZE 7 LEFT
Smith & Nephew, Inc.
71420012
In Commercial Distribution

  • 03596010205483 ()
71420012

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 6 LEFT
Smith & Nephew, Inc.
71420010
In Commercial Distribution

  • 03596010205476 ()
71420010

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 5 LEFT
Smith & Nephew, Inc.
71420008
In Commercial Distribution

  • 03596010205452 ()
71420008

  • Knee arthroplasty wedge
GENESIS II NON POROUS CRUCIATE RETAINING FEMORAL SIZE 4 LEFT
Smith & Nephew, Inc.
71420006
In Commercial Distribution

  • 03596010205445 ()
71420006

  • Knee arthroplasty wedge
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