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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 °, 32mm x 24mm
Altus Spine, LLC
SL32240816
In Commercial Distribution

  • 00843210187143 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240815
In Commercial Distribution

  • 00843210187136 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 8 °, 32mm x 24mm
Altus Spine, LLC
SL32240814
In Commercial Distribution

  • 00843210187129 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272520
In Commercial Distribution

  • 00843210188362 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272519
In Commercial Distribution

  • 00843210188355 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272518
In Commercial Distribution

  • 00843210188348 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272517
In Commercial Distribution

  • 00843210188331 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272516
In Commercial Distribution

  • 00843210188324 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 38mm x 27mm
Altus Spine, LLC
SL38272515
In Commercial Distribution

  • 00843210188317 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 25 °, 32mm x 24mm
Altus Spine, LLC
SL32242520
In Commercial Distribution

  • 00843210188300 ()


  • Polymeric spinal interbody fusion cage
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