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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 °, 32mm x 24mm
Altus Spine, LLC
SL32242019
In Commercial Distribution

  • 00843210159737 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242018
In Commercial Distribution

  • 00843210159720 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242017
In Commercial Distribution

  • 00843210159713 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242016
In Commercial Distribution

  • 00843210159706 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242015
In Commercial Distribution

  • 00843210159690 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242014
In Commercial Distribution

  • 00843210159683 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242013
In Commercial Distribution

  • 00843210159676 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242012
In Commercial Distribution

  • 00843210159669 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 42mm x 30mm
Altus Spine, LLC
SL42301620
In Commercial Distribution

  • 00843210159652 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 16 °, 42mm x 30mm
Altus Spine, LLC
SL42301619
In Commercial Distribution

  • 00843210159645 ()


  • Polymeric spinal interbody fusion cage
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