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, 12x34x28mm 10°SmDeep
Nuvasive, Inc.
1882124
In Commercial Distribution

  • 00887517023452 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x28mm 10°SmDeep
Nuvasive, Inc.
1882123
In Commercial Distribution

  • 00887517023445 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x28mm 10°SmDeep
Nuvasive, Inc.
1882122
In Commercial Distribution

  • 00887517023438 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x28mm 10°SmDeep
Nuvasive, Inc.
1882121
In Commercial Distribution

  • 00887517023421 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x24mm 30° Small
Nuvasive, Inc.
1882120
In Commercial Distribution

  • 00887517023414 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x24mm 30° Small
Nuvasive, Inc.
1882119
In Commercial Distribution

  • 00887517023407 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x24mm 30° Small
Nuvasive, Inc.
1882118
In Commercial Distribution

  • 00887517023391 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x24mm 30° Small
Nuvasive, Inc.
1882117
In Commercial Distribution

  • 00887517023384 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x24mm 25° Small
Nuvasive, Inc.
1882116
In Commercial Distribution

  • 00887517023377 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x24mm 25° Small
Nuvasive, Inc.
1882115
In Commercial Distribution

  • 00887517023360 ()


  • Internal spinal fixation procedure kit, reusable
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