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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,BULLETED TRIAL,6 DEG,17X11
Choice Spine, LP
V070-B61711
In Commercial Distribution

  • 00840996187893 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,6 DEG,17X9
Choice Spine, LP
V070-B61709
In Commercial Distribution

  • 00840996187886 ()


  • Polymeric spinal interbody fusion cage
VEO,BULLETED TRIAL,6 DEG,17X8
Choice Spine, LP
V070-B61708
In Commercial Distribution

  • 00840996187879 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,SHORT,0DEG,17X15
Choice Spine, LP
V070-01715S
In Commercial Distribution

  • 00840996187763 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,SHORT,0DEG,17X13
Choice Spine, LP
V070-01713S
In Commercial Distribution

  • 00840996187756 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,SHORT,0DEG,17X11
Choice Spine, LP
V070-01711S
In Commercial Distribution

  • 00840996187749 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,SHORT,0DEG,17X09
Choice Spine, LP
V070-01709S
In Commercial Distribution

  • 00840996187732 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,SHORT,0DEG,17X08
Choice Spine, LP
V070-01708S
In Commercial Distribution

  • 00840996187725 ()


  • Polymeric spinal interbody fusion cage
VEO,WL CANNULA ADAPTOR
Choice Spine, LP
V070-0017-A1
In Commercial Distribution

  • 00840996185066 ()


  • Polymeric spinal interbody fusion cage
VEO,SLAP HAMMER
Choice Spine, LP
V070-0004ND
In Commercial Distribution

  • 00840996184748 ()


  • Polymeric spinal interbody fusion cage
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