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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Femoral Segment,in combination with Size 4
WALDEMAR LINK GmbH & Co. KG
15-2976/20
In Commercial Distribution

  • 04026575328352 ()
15-2976/20

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 4 LARGE
Smith & Nephew, Inc.
71500042
Not in Commercial Distribution

  • 03596010218155 ()
71500042

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 4 SMALL
Smith & Nephew, Inc.
71500041
Not in Commercial Distribution

  • 03596010218148 ()
71500041

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDFE SIZE 3 LARGE
Smith & Nephew, Inc.
71500032
Not in Commercial Distribution

  • 03596010218117 ()
71500032

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 3 SMALL
Smith & Nephew, Inc.
71500031
Not in Commercial Distribution

  • 03596010218100 ()
71500031

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 2 SMALL
Smith & Nephew, Inc.
71500021
Not in Commercial Distribution

  • 03596010218063 ()
71500021

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE7-8 10MMXSHRT
Smith & Nephew, Inc.
71420712
Not in Commercial Distribution

  • 03596010209054 ()
71420712

  • Knee arthroplasty wedge
GEN II POSTERIOR FEMORAL WEDGE SIZE1-2 5MMXSHORT
Smith & Nephew, Inc.
71420700
Not in Commercial Distribution

  • 03596010208996 ()
71420700

  • Knee arthroplasty wedge
GENESIS II DISTAL FEMORAL WEDGE SIZE7 5MM
Smith & Nephew, Inc.
71420670
Not in Commercial Distribution

  • 03596010208804 ()
71420670

  • Knee arthroplasty wedge
PROFIX POROUS FEMORAL WEDGE SIZE 7 LARGE
Smith & Nephew, Inc.
71500072
Not in Commercial Distribution

  • 03596010218278 ()
71500072

  • Knee arthroplasty wedge
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