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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Archon Plate Bender
Nuvasive, Inc.
8884744
In Commercial Distribution

  • 00887517103178 ()


  • Internal spinal fixation procedure kit, reusable
Universal Probe, Ball-Tip
Nuvasive, Inc.
7459002
In Commercial Distribution

  • 00887517102935 ()


  • Internal spinal fixation procedure kit, reusable
MAS PLIF Screw Loading Block
Nuvasive, Inc.
7070152
In Commercial Distribution

  • 00887517102492 ()


  • Internal spinal fixation procedure kit, reusable
NDI Vicra USB Converter, 4.5m Comm Cable
Nuvasive, Inc.
1583332
In Commercial Distribution

  • 00887517101235 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, Keel Plate
Nuvasive, Inc.
8977360
In Commercial Distribution

  • 00887517100443 ()


  • Internal spinal fixation procedure kit, reusable
Helix Plate Bender
Nuvasive, Inc.
7730701
In Commercial Distribution

  • 00887517089953 ()


  • Internal spinal fixation procedure kit, reusable
Bendini Cable, USB A-B
Nuvasive, Inc.
1583329
In Commercial Distribution

  • 00887517086068 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, In-Situ Left
Nuvasive, Inc.
8977135
In Commercial Distribution

  • 00887517085009 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, In-Situ Right
Nuvasive, Inc.
8977130
In Commercial Distribution

  • 00887517084699 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Bender, Rod
Nuvasive, Inc.
8977110
In Commercial Distribution

  • 00887517084682 ()


  • Internal spinal fixation procedure kit, reusable
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