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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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Modulus - 00887517024121

Modulus ALIF Trial, 10x42x32mm 20° XL
Nuvasive, Inc.
1882191
In Commercial Distribution

  • 00887517024121 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023933

Modulus ALIF Trial, 12x38x30mm 20° Large
Nuvasive, Inc.
1882172
In Commercial Distribution

  • 00887517023933 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023926

Modulus ALIF Trial, 10x38x30mm 20° Large
Nuvasive, Inc.
1882171
In Commercial Distribution

  • 00887517023926 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023919

Modulus ALIF Trial, 8x38x30mm 20° Large
Nuvasive, Inc.
1882170
In Commercial Distribution

  • 00887517023919 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023902

Modulus ALIF Trial, 6x38x30mm 20° Large
Nuvasive, Inc.
1882169
In Commercial Distribution

  • 00887517023902 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023735

Modulus ALIF Trial, 12x38x28mm 20°Medium
Nuvasive, Inc.
1882152
In Commercial Distribution

  • 00887517023735 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023728

Modulus ALIF Trial, 10x38x28mm 20°Medium
Nuvasive, Inc.
1882151
In Commercial Distribution

  • 00887517023728 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023711

Modulus ALIF Trial, 8x38x28mm 20° Medium
Nuvasive, Inc.
1882150
In Commercial Distribution

  • 00887517023711 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023704

Modulus ALIF Trial, 6x38x28mm 20° Medium
Nuvasive, Inc.
1882149
In Commercial Distribution

  • 00887517023704 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023537

Modulus ALIF Trial, 12x34x28mm 20°SmDeep
Nuvasive, Inc.
1882132
In Commercial Distribution

  • 00887517023537 ()


  • Internal spinal fixation procedure kit, reusable
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