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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, 16 degree, 38mmx27mm
Altus Spine, LLC
SL38271616
In Commercial Distribution

  • 00843210187884 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 degree, 38mmx27mm
Altus Spine, LLC
SL38271615
In Commercial Distribution

  • 00843210187877 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 degree, 38mmx27mm
Altus Spine, LLC
SL38271614
In Commercial Distribution

  • 00843210187860 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 degree, 38mmx27mm
Altus Spine, LLC
SL38271613
In Commercial Distribution

  • 00843210187853 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 degree, 38mmx27mm
Altus Spine, LLC
SL38271612
In Commercial Distribution

  • 00843210187846 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 32mm x 24mm
Altus Spine, LLC
SL32241620
In Commercial Distribution

  • 00843210187839 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 32mm x 24mm
Altus Spine, LLC
SL32241619
In Commercial Distribution

  • 00843210187822 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 32mm x 24mm
Altus Spine, LLC
SL32241618
In Commercial Distribution

  • 00843210187815 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 32mm x 24mm
Altus Spine, LLC
SL32241617
In Commercial Distribution

  • 00843210187808 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 32mm x 24mm
Altus Spine, LLC
SL32241616
In Commercial Distribution

  • 00843210187792 ()


  • Polymeric spinal interbody fusion cage
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