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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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LATERAL,TRIAL,0 DEG,17X9
Choice Spine, LP
20-2561
In Commercial Distribution

  • 00840996132886 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,22X15
Choice Spine, LP
20-2231
In Commercial Distribution

  • 00840996132787 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,22X13
Choice Spine, LP
20-2230
In Commercial Distribution

  • 00840996132770 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,22X11
Choice Spine, LP
20-2229
In Commercial Distribution

  • 00840996132763 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,22X9
Choice Spine, LP
20-2228
In Commercial Distribution

  • 00840996132756 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,22X7.5
Choice Spine, LP
V070-02275
In Commercial Distribution

  • 00840996132480 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,22X15
Choice Spine, LP
V070-02215
In Commercial Distribution

  • 00840996132473 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,22X13
Choice Spine, LP
V070-02213
In Commercial Distribution

  • 00840996132466 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,22X11
Choice Spine, LP
V070-02211
In Commercial Distribution

  • 00840996132459 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,22X9
Choice Spine, LP
V070-02209
In Commercial Distribution

  • 00840996132442 ()


  • Polymeric spinal interbody fusion cage
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