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 HL Trial, 12x38x28mm 25°
Nuvasive, Inc.
1982156
In Commercial Distribution

  • 00195377049667 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 10x38x28mm 25°
Nuvasive, Inc.
1982155
In Commercial Distribution

  • 00195377049650 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 8x38x28mm 25°
Nuvasive, Inc.
1982154
In Commercial Distribution

  • 00195377049643 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF HL Trial, 6x38x28mm 25°
Nuvasive, Inc.
1982153
In Commercial Distribution

  • 00195377049636 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x38x28mm 20°Med
Nuvasive, Inc.
1982152
In Commercial Distribution

  • 00195377049629 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 20°Med
Nuvasive, Inc.
1982151
In Commercial Distribution

  • 00195377049612 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x38x28mm 20°Med
Nuvasive, Inc.
1982150
In Commercial Distribution

  • 00195377049605 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x28mm 20°Med
Nuvasive, Inc.
1982149
In Commercial Distribution

  • 00195377049599 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x38x28mm 15°Med
Nuvasive, Inc.
1982148
In Commercial Distribution

  • 00195377049582 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 15°Med
Nuvasive, Inc.
1982147
In Commercial Distribution

  • 00195377049575 ()


  • Internal spinal fixation procedure kit, reusable
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