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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RELINE Attachment, Tower Handle VBD2
Nuvasive, Inc.
11000718
In Commercial Distribution

  • 00887517024466 ()


  • Internal spinal fixation procedure kit, reusable
RELINE Handle, Quick Connect VBD2
Nuvasive, Inc.
11000717
In Commercial Distribution

  • 00887517024459 ()


  • Surgical instrument handle, non-torque-limiting
RELINE Clamp, En Bloc VBD2
Nuvasive, Inc.
11000714
In Commercial Distribution

  • 00887517024428 ()


  • Internal spinal fixation procedure kit, reusable
RELINE Segmental Rack, VBD2
Nuvasive, Inc.
11000712
In Commercial Distribution

  • 00887517024404 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Awl, Straight
Nuvasive, Inc.
D1882042
In Commercial Distribution

  • 00887517024282 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 10x42x32mm 30° XL
Nuvasive, Inc.
1882199
In Commercial Distribution

  • 00887517024206 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 6x42x32mm 30° XL
Nuvasive, Inc.
1882197
In Commercial Distribution

  • 00887517024183 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x42x32mm 25° XL
Nuvasive, Inc.
1882196
In Commercial Distribution

  • 00887517024176 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 8x42x32mm 25° XL
Nuvasive, Inc.
1882194
In Commercial Distribution

  • 00887517024152 ()


  • Internal spinal fixation procedure kit, reusable
Modulus ALIF Trial, 12x42x32mm 20° XL
Nuvasive, Inc.
1882192
In Commercial Distribution

  • 00887517024138 ()


  • Internal spinal fixation procedure kit, reusable
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