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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 °, 38mm x 27mm
Altus Spine, LLC
SL38270819
In Commercial Distribution

  • 00843210187297 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270818
In Commercial Distribution

  • 00843210187280 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270817
In Commercial Distribution

  • 00843210187273 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270816
In Commercial Distribution

  • 00843210187266 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270815
In Commercial Distribution

  • 00843210187259 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270814
In Commercial Distribution

  • 00843210187242 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270813
In Commercial Distribution

  • 00843210187235 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270812
In Commercial Distribution

  • 00843210187228 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 38mm x 27mm
Altus Spine, LLC
SL38270811
In Commercial Distribution

  • 00843210187211 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240820
In Commercial Distribution

  • 00843210187181 ()


  • Polymeric spinal interbody fusion cage
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