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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Modulus ALIF Trial, 12x38x30mm 15° Large
Nuvasive, Inc.
1882168
In Commercial Distribution

  • 00887517023896 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x30mm 15° Large
Nuvasive, Inc.
1882167
In Commercial Distribution

  • 00887517023889 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x30mm 15° Large
Nuvasive, Inc.
1882165
In Commercial Distribution

  • 00887517023865 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x30mm 10° Large
Nuvasive, Inc.
1882163
In Commercial Distribution

  • 00887517023841 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x30mm 10° Large
Nuvasive, Inc.
1882161
In Commercial Distribution

  • 00887517023827 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 30°Medium
Nuvasive, Inc.
1882159
In Commercial Distribution

  • 00887517023803 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x28mm 30° Medium
Nuvasive, Inc.
1882157
In Commercial Distribution

  • 00887517023780 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 25°Medium
Nuvasive, Inc.
1882155
In Commercial Distribution

  • 00887517023766 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x28mm 20° Medium
Nuvasive, Inc.
1882149
In Commercial Distribution

  • 00887517023704 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 15°Medium
Nuvasive, Inc.
1882147
In Commercial Distribution

  • 00887517023681 ()


  • Internal spinal fixation procedure kit, reusable
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