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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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BLACKHAWK TI,LOR,STERILE,14WX12DX6H
Choice Spine, LP
S-TT20-1412606
In Commercial Distribution

  • 00840996186452 ()


  • Polymeric spinal interbody fusion cage
BLACKHAWK TI,LOR,STERILE,14WX12DX5H
Choice Spine, LP
S-TT20-1412605
In Commercial Distribution

  • 00840996186445 ()


  • 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
VEO,RASPING PADDLE.ANGLED,LARGE
Choice Spine, LP
V070-A0106RPL
In Commercial Distribution

  • 00840996184397 ()


  • Polymeric spinal interbody fusion cage
VEORASPING,PADDLE,ANGLED,LARGE
Choice Spine, LP
V070-A010XRPL
In Commercial Distribution

  • 00840996184380 ()


  • Polymeric spinal interbody fusion cage
ASCENDANT,TRIAL-RASP,LR,NS,14X16X12
Choice Spine, LP
05-099-31-1612N
In Commercial Distribution

  • 00840996184373 ()


  • Polymeric spinal interbody fusion cage
ASCENDANT,TRIAL-RASP,LR,NS,14X16X11
Choice Spine, LP
05-099-31-1611N
In Commercial Distribution

  • 00840996184366 ()


  • Polymeric spinal interbody fusion cage
ASCENDANT,TRIAL-RASP,LR,NS,14X16X10
Choice Spine, LP
05-099-31-1610N
In Commercial Distribution

  • 00840996184359 ()


  • Polymeric spinal interbody fusion cage
ASCENDANT,TRIAL-RASP,LR,NS,14X16X9
Choice Spine, LP
05-099-31-1609N
In Commercial Distribution

  • 00840996184342 ()


  • Polymeric spinal interbody fusion cage
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