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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, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242518
In Commercial Distribution

  • 00843210160016 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242517
In Commercial Distribution

  • 00843210160009 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242516
In Commercial Distribution

  • 00843210159997 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242515
In Commercial Distribution

  • 00843210159980 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242514
In Commercial Distribution

  • 00843210159973 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302020
In Commercial Distribution

  • 00843210159966 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302019
In Commercial Distribution

  • 00843210159959 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302018
In Commercial Distribution

  • 00843210159942 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302017
In Commercial Distribution

  • 00843210159935 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 42mm x 30mm
Altus Spine, LLC
SL42302016
In Commercial Distribution

  • 00843210159928 ()


  • Polymeric spinal interbody fusion cage
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