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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DBR® III Screw, 7.5x30mm Cannulated
Nuvasive, Inc.
4487530
In Commercial Distribution

  • 00887517223616 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR III Screw, 6.5x60mm Cannulated
Nuvasive, Inc.
4486560
In Commercial Distribution

  • 00887517219374 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x55mm Cannulated
Nuvasive, Inc.
4486555
In Commercial Distribution

  • 00887517219367 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x50mm Cannulated
Nuvasive, Inc.
4486550
In Commercial Distribution

  • 00887517219350 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x45mm Cannulated
Nuvasive, Inc.
4486545
In Commercial Distribution

  • 00887517219343 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x40mm Cannulated
Nuvasive, Inc.
4486540
In Commercial Distribution

  • 00887517219336 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x35mm Cannulated
Nuvasive, Inc.
4486535
In Commercial Distribution

  • 00887517219329 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR® III Screw, 6.5x30mm Cannulated
Nuvasive, Inc.
4486530
In Commercial Distribution

  • 00887517219312 ()


  • Bone-screw internal spinal fixation system, non-sterile
DBR III MOD Implant/Instrument Tray Base
Nuvasive, Inc.
7280103
In Commercial Distribution

  • 00887517215949 ()


  • Device sterilization/disinfection container, reusable
DBR® III Screw, 5.5x55mm Cannulated
Nuvasive, Inc.
4485555
In Commercial Distribution

  • 00887517215291 ()


  • Bone-screw internal spinal fixation system, non-sterile
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