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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, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272020
In Commercial Distribution

  • 00843210159904 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272019
In Commercial Distribution

  • 00843210159898 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272018
In Commercial Distribution

  • 00843210159881 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272017
In Commercial Distribution

  • 00843210159874 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272016
In Commercial Distribution

  • 00843210159867 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272015
In Commercial Distribution

  • 00843210159850 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272014
In Commercial Distribution

  • 00843210159843 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 38mm x 27mm
Altus Spine, LLC
SL38272013
In Commercial Distribution

  • 00843210159836 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242020
In Commercial Distribution

  • 00843210159744 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242019
In Commercial Distribution

  • 00843210159737 ()


  • Polymeric spinal interbody fusion cage
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