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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, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271218
In Commercial Distribution

  • 00843210187617 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271217
In Commercial Distribution

  • 00843210187600 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271216
In Commercial Distribution

  • 00843210187594 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271215
In Commercial Distribution

  • 00843210187587 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271214
In Commercial Distribution

  • 00843210187570 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 degree, 38mm x 27mm
Altus Spine, LLC
SL38271213
In Commercial Distribution

  • 00843210187563 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 38mm x 27mm
Altus Spine, LLC
SL38271211
In Commercial Distribution

  • 00843210187556 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 32mm x 24mm
Altus Spine, LLC
SL32241220
In Commercial Distribution

  • 00843210187532 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 32mm x 24mm
Altus Spine, LLC
SL32241219
In Commercial Distribution

  • 00843210187525 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 32mm x 24mm
Altus Spine, LLC
SL32241218
In Commercial Distribution

  • 00843210187518 ()


  • Polymeric spinal interbody fusion cage
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