SEARCH RESULTS FOR: Femoral(4163 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 Class Implantable

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SpheriKA Femoral Trial with Lugs S2L
Medacta International SA
02.12.10.2995
In Commercial Distribution

  • 07630542755019 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
SpheriKA Femoral Trial with Lugs S1R
Medacta International SA
02.12.10.2992
In Commercial Distribution

  • 07630542754982 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
SpheriKA Femoral Trial with Lugs S1L
Medacta International SA
02.12.10.2991
In Commercial Distribution

  • 07630542754975 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Femoral Posterior Augmentation # 6/5mm - Ti6Al4V
Medacta International SA
02.07.7605FPW
In Commercial Distribution

  • 07630040721745 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 5/10mm - Ti6Al4V
Medacta International SA
02.07.7510FPW
In Commercial Distribution

  • 07630040721691 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 5/5mm - Ti6Al4V
Medacta International SA
02.07.7505FPW
In Commercial Distribution

  • 07630040721677 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 4/10mm - Ti6Al4V
Medacta International SA
02.07.7410FPW
In Commercial Distribution

  • 07630040721622 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 3/10mm - Ti6Al4V
Medacta International SA
02.07.7310FPW
In Commercial Distribution

  • 07630040721554 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 3/5mm - Ti6Al4V
Medacta International SA
02.07.7305FPW
In Commercial Distribution

  • 07630040721530 ()


  • Knee arthroplasty wedge
Femoral Posterior Augmentation # 2/5mm - Ti6Al4V
Medacta International SA
02.07.7205FPW
In Commercial Distribution

  • 07630040721462 ()


  • Knee arthroplasty wedge
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