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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 °, 32mm x 24mm
Altus Spine, LLC
SL32241212
In Commercial Distribution

  • 00843210187457 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 12 degree, 32mmx24mm
Altus Spine, LLC
SL32241211
In Commercial Distribution

  • 00843210187440 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300820
In Commercial Distribution

  • 00843210187419 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300819
In Commercial Distribution

  • 00843210187402 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300818
In Commercial Distribution

  • 00843210187396 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300817
In Commercial Distribution

  • 00843210187389 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300816
In Commercial Distribution

  • 00843210187372 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300815
In Commercial Distribution

  • 00843210187365 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300814
In Commercial Distribution

  • 00843210187358 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 42mm x 30mm
Altus Spine, LLC
SL42300813
In Commercial Distribution

  • 00843210187341 ()


  • Polymeric spinal interbody fusion cage
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