SEARCH RESULTS FOR: (*Buy Two Internal Territory Driver*)(76862 results)

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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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NA - 03663136024387

Angled ring left
SPINEVISION
TL1-A018-1
In Commercial Distribution

  • 03663136024387 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024370

Angled curette right
SPINEVISION
TL1-A017-2
In Commercial Distribution

  • 03663136024370 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024363

Angled curette left
SPINEVISION
TL1-A017-1
In Commercial Distribution

  • 03663136024363 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024356

Straight rack curette
SPINEVISION
TL1-A016
In Commercial Distribution

  • 03663136024356 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024349

Bone tamp - straight
SPINEVISION
TL1-A015-3
In Commercial Distribution

  • 03663136024349 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024332

Bone tamp - curved
SPINEVISION
TL1-A015-2
In Commercial Distribution

  • 03663136024332 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024325

Bone tamp - angled
SPINEVISION
TL1-A015-1
In Commercial Distribution

  • 03663136024325 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024318

Straight scraper
SPINEVISION
TL1-A014
In Commercial Distribution

  • 03663136024318 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024301

Final Impactor
SPINEVISION
TL1-A013
In Commercial Distribution

  • 03663136024301 ()

  • 0


  • Polymeric spinal interbody fusion cage

NA - 03663136024295

Nerve Root Retractor/T
SPINEVISION
TL1-A012
In Commercial Distribution

  • 03663136024295 ()

  • 0


  • Polymeric spinal interbody fusion cage
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