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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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PRECEPT Screw, 5.0x35mm Polyaxial TL
Nuvasive, Inc.
8835035A
In Commercial Distribution

  • 00887517394224 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 5.0x30mm Polyaxial TL
Nuvasive, Inc.
8835030B
In Commercial Distribution

  • 00887517394217 ()


  • Bone-screw internal spinal fixation system, non-sterile
PRECEPT Screw, 5.0x30mm Polyaxial TL
Nuvasive, Inc.
8835030A
In Commercial Distribution

  • 00887517394200 ()


  • Bone-screw internal spinal fixation system, non-sterile
CoRoent XLR-F, 14x34x24 8°
Nuvasive, Inc.
6921434
In Commercial Distribution

  • 00887517394187 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XLR, 12x38x28 8°
Nuvasive, Inc.
6921288
In Commercial Distribution

  • 00887517394149 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 12x22x60mm Lordotic
Nuvasive, Inc.
6921260
In Commercial Distribution

  • 00887517394132 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 12x22x55mm Lordotic
Nuvasive, Inc.
6921255
In Commercial Distribution

  • 00887517394125 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 12x22x50mm Lordotic
Nuvasive, Inc.
6921250
In Commercial Distribution

  • 00887517394118 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL Wide, 12x22x45mm Lordotic
Nuvasive, Inc.
6921245
In Commercial Distribution

  • 00887517394101 ()


  • Polymeric spinal interbody fusion cage
PRECEPT Screw, 5.0x25mm Polyaxial TL
Nuvasive, Inc.
8835025B
In Commercial Distribution

  • 00887517393890 ()


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