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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 °, 42mm x 30mm
Altus Spine, LLC
SL42301220
In Commercial Distribution

  • 00843210187730 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301219
In Commercial Distribution

  • 00843210187723 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301218
In Commercial Distribution

  • 00843210187716 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301217
In Commercial Distribution

  • 00843210187709 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301216
In Commercial Distribution

  • 00843210187693 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301215
In Commercial Distribution

  • 00843210187686 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301214
In Commercial Distribution

  • 00843210187679 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301213
In Commercial Distribution

  • 00843210187662 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301212
In Commercial Distribution

  • 00843210187655 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 °, 42mm x 30mm
Altus Spine, LLC
SL42301211
In Commercial Distribution

  • 00843210187648 ()


  • Polymeric spinal interbody fusion cage
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