SEARCH RESULTS FOR: Femoral(124689 results)

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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 Distal Augmentation # 2/4mm-Ti6Al4V
Medacta International SA
02.07.7204FDW
In Commercial Distribution

  • 07630040721455 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation# 1/20mm-Ti6Al4V
Medacta International SA
02.07.7120FDA
In Commercial Distribution

  • 07630040721448 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation# 1/16mm-Ti6Al4V
Medacta International SA
02.07.7116FDA
In Commercial Distribution

  • 07630040721431 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation# 1/12mm-Ti6Al4V
Medacta International SA
02.07.7112FDA
In Commercial Distribution

  • 07630040721424 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation # 1/8mm-Ti6Al4V
Medacta International SA
02.07.7108FDW
In Commercial Distribution

  • 07630040721400 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation # 1/4mm-Ti6Al4V
Medacta International SA
02.07.7104FDW
In Commercial Distribution

  • 07630040721387 ()


  • Knee arthroplasty wedge
BUCK FEMORAL CEMENT RESTRICTOR 18.5MM
Smith & Nephew, Inc.
129418
In Commercial Distribution

  • 23596010086437 ()
  • 03596010086433 ()
129418

  • Polymer orthopaedic cement restrictor, non-bioabsorbable
GENISIS UNI FEMORAL MAGNUM PLUS
Smith & Nephew, Inc.
71245007
In Commercial Distribution

  • 03596010188519 ()
71245007

  • Uncoated unicondylar knee femur prosthesis
Size 6 Right Femoral PS
Novosource, LLC
3101-2206
In Commercial Distribution

  • 00811382031960 ()

  • 6
3101-2206

  • Posterior-stabilized total knee prosthesis
Size 5 Right Femoral PS
Novosource, LLC
3101-2205
In Commercial Distribution

  • 00811382031953 ()

  • 5
3101-2205

  • Posterior-stabilized total knee prosthesis
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