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

  • 00887517023711 ()


  • 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, 12x34x28mm 20°SmDeep
Nuvasive, Inc.
1882132
In Commercial Distribution

  • 00887517023537 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x28mm 20°SmDeep
Nuvasive, Inc.
1882131
In Commercial Distribution

  • 00887517023520 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x28mm 20°SmDeep
Nuvasive, Inc.
1882130
In Commercial Distribution

  • 00887517023513 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x28mm 20°SmDeep
Nuvasive, Inc.
1882129
In Commercial Distribution

  • 00887517023506 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x24mm 20° Small
Nuvasive, Inc.
1882112
In Commercial Distribution

  • 00887517023339 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x24mm 20° Small
Nuvasive, Inc.
1882111
In Commercial Distribution

  • 00887517023322 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x24mm 20° Small
Nuvasive, Inc.
1882110
In Commercial Distribution

  • 00887517023315 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x24mm 20° Small
Nuvasive, Inc.
1882109
In Commercial Distribution

  • 00887517023308 ()


  • Internal spinal fixation procedure kit, reusable
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