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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 Size Type Device Class Implantable

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XLIF AMS Plate, 12mm Dual-Sided
Nuvasive, Inc.
1910212P2
In Commercial Distribution

  • 00195377016959 ()


  • Polymeric spinal interbody fusion cage
XLIF AMS Plate, 10mm Dual-Sided
Nuvasive, Inc.
1910210P2
In Commercial Distribution

  • 00195377016942 ()


  • Polymeric spinal interbody fusion cage
XLIF AMS Plate, 8mm Dual-Sided
Nuvasive, Inc.
1910208P2
In Commercial Distribution

  • 00195377016935 ()


  • Polymeric spinal interbody fusion cage
XLIF AMS Plate, 12mm Single-Sided
Nuvasive, Inc.
1910112P2
In Commercial Distribution

  • 00195377016928 ()


  • Polymeric spinal interbody fusion cage
XLIF AMS Plate, 10mm Single-Sided
Nuvasive, Inc.
1910110P2
In Commercial Distribution

  • 00195377016911 ()


  • Polymeric spinal interbody fusion cage
XLIF AMS Plate, 8mm Single-Sided
Nuvasive, Inc.
1910108P2
In Commercial Distribution

  • 00195377016904 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 6x14x12mm 7°
Nuvasive, Inc.
4061427P2
In Commercial Distribution

  • 00195377006813 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 6x16x14mm 7°
Nuvasive, Inc.
4061647P2
In Commercial Distribution

  • 00195377006806 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 7x14x12mm 7°
Nuvasive, Inc.
4071427P2
In Commercial Distribution

  • 00195377006790 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 7x16x14mm 7°
Nuvasive, Inc.
4071647P2
In Commercial Distribution

  • 00195377006783 ()


  • Polymeric spinal interbody fusion cage
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