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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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OCTANE M,RATCHET INSERTER HANDLE
Choice Spine, LP
05-049-03-0000
In Commercial Distribution

  • 00840996153454 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,INSERTER, INNER WEDGE
Choice Spine, LP
05-099-01-0006
In Commercial Distribution

  • 00840996153263 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,INSERTER
Choice Spine, LP
05-099-01-0000
In Commercial Distribution

  • 00840996153256 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,SINGLE IMPACTOR
Choice Spine, LP
05-099-44-2000
In Commercial Distribution

  • 00840996153041 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,CURETTE,STRT RING
Choice Spine, LP
05-099-14-0000
In Commercial Distribution

  • 00840996152945 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,DOMED RASP NO STOP
Choice Spine, LP
05-099-12-0000
In Commercial Distribution

  • 00840996152921 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,ANGLE RASP N/S KNURL
Choice Spine, LP
05-099-11-0002
In Commercial Distribution

  • 00840996152907 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,ANGLED RASP NO STOP
Choice Spine, LP
05-099-11-0000
In Commercial Distribution

  • 00840996152884 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,DM,WS,14X16X7
Choice Spine, LP
05-099-29-1607
In Commercial Distribution

  • 00840996152624 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,DM,WS,14X16X6
Choice Spine, LP
05-099-29-1606
In Commercial Distribution

  • 00840996152617 ()


  • Polymeric spinal interbody fusion cage
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