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, 6x38x28mm 15° Medium
Nuvasive, Inc.
1882145
In Commercial Distribution

  • 00887517023667 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x38x28mm 10°Medium
Nuvasive, Inc.
1882143
In Commercial Distribution

  • 00887517023643 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x38x28mm 10° Medium
Nuvasive, Inc.
1882141
In Commercial Distribution

  • 00887517023629 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x28mm 30°SmDeep
Nuvasive, Inc.
1882139
In Commercial Distribution

  • 00887517023605 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x28mm 30°SmDeep
Nuvasive, Inc.
1882137
In Commercial Distribution

  • 00887517023582 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x34x28mm 25°SmDeep
Nuvasive, Inc.
1882136
In Commercial Distribution

  • 00887517023575 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x34x28mm 25°SmDeep
Nuvasive, Inc.
1882135
In Commercial Distribution

  • 00887517023568 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x34x28mm 25°SmDeep
Nuvasive, Inc.
1882134
In Commercial Distribution

  • 00887517023551 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x34x28mm 25°SmDeep
Nuvasive, Inc.
1882133
In Commercial Distribution

  • 00887517023544 ()


  • 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
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