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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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VEO,ANGLED TRIAL,POLISHED,0 DEG,17X11
Choice Spine, LP
V070-A1711P
In Commercial Distribution

  • 00840996170444 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,17X9
Choice Spine, LP
V070-A1709P
In Commercial Distribution

  • 00840996170437 ()


  • Polymeric spinal interbody fusion cage
VEO,ANGLED TRIAL,POLISHED,0 DEG,17X7.5
Choice Spine, LP
V070-A1775P
In Commercial Distribution

  • 00840996170420 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,22X15
Choice Spine, LP
V070-62215P
In Commercial Distribution

  • 00840996170413 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,22X13
Choice Spine, LP
V070-62213P
In Commercial Distribution

  • 00840996170406 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,22X11
Choice Spine, LP
V070-62211P
In Commercial Distribution

  • 00840996170390 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,22X9
Choice Spine, LP
V070-62209P
In Commercial Distribution

  • 00840996170383 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,22X8
Choice Spine, LP
V070-62208P
In Commercial Distribution

  • 00840996170376 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,17X15
Choice Spine, LP
V070-61715P
In Commercial Distribution

  • 00840996170369 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,POLISHED,6 DEG,17X13
Choice Spine, LP
V070-61713P
In Commercial Distribution

  • 00840996170352 ()


  • Polymeric spinal interbody fusion cage
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