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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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Cervical IBF PEEK-HA, 14x11x4mm, 0 degree
VY SPINE LLC
1-02-004HA
In Commercial Distribution

  • 00842566100189 ()
1-02-004HA

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x11, 7 Deg
VY SPINE LLC
1-01-711
In Commercial Distribution

  • 00842566100165 ()
1-01-711

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x10, 7 Deg
VY SPINE LLC
1-01-710
In Commercial Distribution

  • 00842566100158 ()
1-01-710

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x9, 7 Deg
VY SPINE LLC
1-01-709
In Commercial Distribution

  • 00842566100141 ()
1-01-709

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x8, 7 Deg
VY SPINE LLC
1-01-708
In Commercial Distribution

  • 00842566100134 ()
1-01-708

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x7, 7 Deg
VY SPINE LLC
1-01-707
In Commercial Distribution

  • 00842566100127 ()
1-01-707

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x6, 7 Deg
VY SPINE LLC
1-01-706
In Commercial Distribution

  • 00842566100110 ()
1-01-706

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x5, 7 Deg
VY SPINE LLC
1-01-705
In Commercial Distribution

  • 00842566100103 ()
1-01-705

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x4, 7 Deg
VY SPINE LLC
1-01-704
In Commercial Distribution

  • 00842566100097 ()
1-01-704

  • Polymeric spinal interbody fusion cage
IBF, Peek Optima HA Enhanced, 12x10x11, 0 Deg
VY SPINE LLC
1-01-011HA
In Commercial Distribution

  • 00842566100080 ()
1-01-011HA

  • Polymeric spinal interbody fusion cage
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