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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, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242020
In Commercial Distribution

  • 00843210159744 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242019
In Commercial Distribution

  • 00843210159737 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242018
In Commercial Distribution

  • 00843210159720 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242017
In Commercial Distribution

  • 00843210159713 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242016
In Commercial Distribution

  • 00843210159706 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242015
In Commercial Distribution

  • 00843210159690 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242014
In Commercial Distribution

  • 00843210159683 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242013
In Commercial Distribution

  • 00843210159676 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242012
In Commercial Distribution

  • 00843210159669 ()


  • Polymeric spinal interbody fusion cage
BLUNT BLADE 20 x 85 MM, SILVER
TEDAN SURGICAL INNOVATIONS, L.L.C.
CS-4041
In Commercial Distribution

  • 00843059121841 ()


  • Surgical retractor/retraction system blade, reusable
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