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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 - 00887517023520

Modulus ALIF Trial, 10x34x28mm 20°SmDeep
Nuvasive, Inc.
1882131
In Commercial Distribution

  • 00887517023520 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023513

Modulus ALIF Trial, 8x34x28mm 20°SmDeep
Nuvasive, Inc.
1882130
In Commercial Distribution

  • 00887517023513 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023506

Modulus ALIF Trial, 6x34x28mm 20°SmDeep
Nuvasive, Inc.
1882129
In Commercial Distribution

  • 00887517023506 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023339

Modulus ALIF Trial, 12x34x24mm 20° Small
Nuvasive, Inc.
1882112
In Commercial Distribution

  • 00887517023339 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023322

Modulus ALIF Trial, 10x34x24mm 20° Small
Nuvasive, Inc.
1882111
In Commercial Distribution

  • 00887517023322 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023315

Modulus ALIF Trial, 8x34x24mm 20° Small
Nuvasive, Inc.
1882110
In Commercial Distribution

  • 00887517023315 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517023308

Modulus ALIF Trial, 6x34x24mm 20° Small
Nuvasive, Inc.
1882109
In Commercial Distribution

  • 00887517023308 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517024114

Modulus ALIF Trial, 8x42x32mm 20° XL
Nuvasive, Inc.
1882190
In Commercial Distribution

  • 00887517024114 ()


  • Internal spinal fixation procedure kit, reusable

Modulus - 00887517024107

Modulus ALIF Trial, 6x42x32mm 20° XL
Nuvasive, Inc.
1882189
In Commercial Distribution

  • 00887517024107 ()


  • 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
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