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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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ACAPELLA,TRIAL,LR,WS,12X14X9
Choice Spine, LP
05-099-27-1409
In Commercial Distribution

  • 00840996152037 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,LR,WS,12X14X7
Choice Spine, LP
05-099-27-1407
In Commercial Distribution

  • 00840996152013 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,LR,WS,12X14X5
Choice Spine, LP
05-099-27-1405
In Commercial Distribution

  • 00840996151993 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,A1 SINGLE IMPACTOR
Choice Spine, LP
05-099-08-0000
In Commercial Distribution

  • 00840996151979 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,CX,WS,14X16X12
Choice Spine, LP
05-099-33-1612
In Commercial Distribution

  • 00840996151955 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,DM,WS,14X16X10
Choice Spine, LP
05-099-33-1610
In Commercial Distribution

  • 00840996151931 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,DM,WS,14X16X8
Choice Spine, LP
05-099-33-1608
In Commercial Distribution

  • 00840996151917 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,DM,WS,14X16X6
Choice Spine, LP
05-099-33-1606
In Commercial Distribution

  • 00840996151894 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,CX,WS,12X14X12
Choice Spine, LP
05-099-33-1412
In Commercial Distribution

  • 00840996151870 ()


  • Polymeric spinal interbody fusion cage
ACAPELLA,TRIAL,RASP,DM,WS,12X14X10
Choice Spine, LP
05-099-33-1410
In Commercial Distribution

  • 00840996151856 ()


  • Polymeric spinal interbody fusion cage
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