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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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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
IBF, Peek 12x10x11, 0 Deg
VY SPINE LLC
1-01-011
In Commercial Distribution

  • 00842566100073 ()
1-01-011

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x10, 0 Deg
VY SPINE LLC
1-01-010
In Commercial Distribution

  • 00842566100066 ()
1-01-010

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x9, 0 Deg
VY SPINE LLC
1-01-009
In Commercial Distribution

  • 00842566100059 ()
1-01-009

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x8, 0 Deg
VY SPINE LLC
1-01-008
In Commercial Distribution

  • 00842566100042 ()
1-01-008

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x7, 0 Deg
VY SPINE LLC
1-01-007
In Commercial Distribution

  • 00842566100035 ()
1-01-007

  • Polymeric spinal interbody fusion cage
IBF, Peek 12x10x6, 0 Deg
VY SPINE LLC
1-01-006
In Commercial Distribution

  • 00842566100028 ()
1-01-006

  • Polymeric spinal interbody fusion cage
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