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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
SL32241213
In Commercial Distribution

  • 00843210187464 ()


  • Polymeric spinal interbody fusion cage
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
Titanium Interbody, 12 degree, 38mmx27mm
Altus Spine, LLC
SL38271211T
In Commercial Distribution

  • 00843210181332 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 12 degree, 38mmx27mm
Altus Spine, LLC
SL38271212T
In Commercial Distribution

  • 00843210181325 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 12 degree, 38mmx27mm
Altus Spine, LLC
SL38271213T
In Commercial Distribution

  • 00843210181318 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 8 degree, 42mmx30mm
Altus Spine, LLC
SL42300819T
In Commercial Distribution

  • 00843210180472 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 12 degree, 42mmx30mm
Altus Spine, LLC
SL42301211T
In Commercial Distribution

  • 00843210180434 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 12 degree, 42mmx30mm
Altus Spine, LLC
SL42301214T
In Commercial Distribution

  • 00843210180373 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 12 degree, 42mmx30mm
Altus Spine, LLC
SL42301215T
In Commercial Distribution

  • 00843210180366 ()


  • Polymeric spinal interbody fusion cage
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