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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 Size Device Class Implantable

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CoRoent SI Screwdriver, 2.5mm
Nuvasive, Inc.
6780118
In Commercial Distribution

  • 00887517356178 ()


  • Surgical screwdriver, reusable
CoRoent SI Screwdriver, 2.5mm
Nuvasive, Inc.
6780117
In Commercial Distribution

  • 00887517356161 ()


  • Surgical screwdriver, reusable
CoRoent Small Interlock Screwdriver
Nuvasive, Inc.
6780111
In Commercial Distribution

  • 00887517356109 ()


  • Surgical screwdriver, reusable
PRECEPT Screw, 5.5x55mm Polyaxial
Nuvasive, Inc.
8805555
In Commercial Distribution

  • 00887517355980 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 5.5x50mm Polyaxial
Nuvasive, Inc.
8805550
In Commercial Distribution

  • 00887517355973 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 5.5x45mm Polyaxial
Nuvasive, Inc.
8805545
In Commercial Distribution

  • 00887517355966 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 5.5x40mm Polyaxial
Nuvasive, Inc.
8805540
In Commercial Distribution

  • 00887517355959 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 70mm Pre-Bent
Nuvasive, Inc.
7217070
In Commercial Distribution

  • 00887517433404 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 65mm Pre-Bent
Nuvasive, Inc.
7217065
In Commercial Distribution

  • 00887517433091 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR® III Rod, 60mm Pre-Bent
Nuvasive, Inc.
7217060
In Commercial Distribution

  • 00887517433084 ()


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