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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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PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240819
In Commercial Distribution

  • 00843210187174 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240818
In Commercial Distribution

  • 00843210187167 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240817
In Commercial Distribution

  • 00843210187150 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240816
In Commercial Distribution

  • 00843210187143 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240815
In Commercial Distribution

  • 00843210187136 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240814
In Commercial Distribution

  • 00843210187129 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240813
In Commercial Distribution

  • 00843210187112 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240812
In Commercial Distribution

  • 00843210187105 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240811
In Commercial Distribution

  • 00843210187099 ()


  • Polymeric spinal interbody fusion cage
32mm x 24mm, 8°, 9mm PEEK Spacer
Altus Spine, LLC
FA32240809
In Commercial Distribution

  • 00843210185538 ()


  • Polymeric spinal interbody fusion cage
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