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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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Reliance IBF-VBS PEEK 10x26x10, 0°
VY SPINE LLC
1-05-010
In Commercial Distribution

  • 00842566100547 ()
1-05-010

  • Polymeric spinal interbody fusion cage
Reliance IBF-VBS PEEK 10x26x9, 0°
VY SPINE LLC
1-05-009
In Commercial Distribution

  • 00842566100530 ()
1-05-009

  • Polymeric spinal interbody fusion cage
Reliance IBF-VBS PEEK 10x26x8, 0°
VY SPINE LLC
1-05-008
In Commercial Distribution

  • 00842566100523 ()
1-05-008

  • Polymeric spinal interbody fusion cage
Reliance IBF-VBS PEEK 10x26x7, 0°
VY SPINE LLC
1-05-007
In Commercial Distribution

  • 00842566100516 ()
1-05-007

  • Polymeric spinal interbody fusion cage
Reliance IBF-VBS PEEK 10x26x6, 0°
VY SPINE LLC
1-05-006
In Commercial Distribution

  • 00842566100509 ()
1-05-006

  • 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
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