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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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Interlock II Ti-C, 9x19x16mm 20°
Nuvasive, Inc.
6778920CP2
In Commercial Distribution

  • 00887517813282 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 16x17x14mm 20°
Nuvasive, Inc.
6771620CP2
In Commercial Distribution

  • 00887517812902 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 15x17x14mm 20°
Nuvasive, Inc.
6771520CP2
In Commercial Distribution

  • 00887517812841 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 14x17x14mm 20°
Nuvasive, Inc.
6771420CP2
In Commercial Distribution

  • 00887517812780 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 13x17x14mm 20°
Nuvasive, Inc.
6771320CP2
In Commercial Distribution

  • 00887517812728 ()


  • Polymeric spinal interbody fusion cage
42X 30X 19mm X 20° PEEK-2C
PRECISION SPINE, INC.
69-AV-2019-2C
Not in Commercial Distribution

  • 00840019963909 ()
69-AV-2019-2C

  • Polymeric spinal interbody fusion cage
42X 30X 17mm X 20° PEEK-2C
PRECISION SPINE, INC.
69-AV-2017-2C
Not in Commercial Distribution

  • 00840019963893 ()
69-AV-2017-2C

  • Polymeric spinal interbody fusion cage
42X 30X 15mm X 20° PEEK-2C
PRECISION SPINE, INC.
69-AV-2015-2C
Not in Commercial Distribution

  • 00840019963886 ()
69-AV-2015-2C

  • Polymeric spinal interbody fusion cage
42X 30X 13mm X 20° PEEK-2C
PRECISION SPINE, INC.
69-AV-2013-2C
Not in Commercial Distribution

  • 00840019963879 ()
69-AV-2013-2C

  • Polymeric spinal interbody fusion cage
42X 30X 19mm X 20° PEEK
PRECISION SPINE, INC.
69-AV-2019
In Commercial Distribution

  • 00840019962704 ()
69-AV-2019

  • Polymeric spinal interbody fusion cage
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