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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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Lumbar Cage, 21 x 16mm, 0° NT
Kalitec Direct LLC
12-PCN-2116
In Commercial Distribution

  • B07312PCN21160 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage, 21 x 15mm, 0° NT
Kalitec Direct LLC
12-PCN-2115
In Commercial Distribution

  • B07312PCN21150 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage, 21 x 14mm, 0° NT
Kalitec Direct LLC
12-PCN-2114
In Commercial Distribution

  • B07312PCN21140 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage, 21 x 13mm, 0° NT
Kalitec Direct LLC
12-PCN-2113
In Commercial Distribution

  • B07312PCN21130 ()


  • Polymeric spinal interbody fusion cage
Cage, 21 x 11mm, 0 Degree, No Taper, Straight
Kalitec Direct LLC
12-PCN-2111
In Commercial Distribution

  • B07312PCN21110 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage, 21 x 10mm, 0° NT
Kalitec Direct LLC
12-PCN-2110
In Commercial Distribution

  • B07312PCN21100 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage, 21 x 9mm, 0° NT
Kalitec Direct LLC
12-PCN-2109
In Commercial Distribution

  • B07312PCN21090 ()


  • Polymeric spinal interbody fusion cage
Lumbar Cage,, 21 X 8mm, 0° NT
Kalitec Direct LLC
12-PCN-2108
In Commercial Distribution

  • B07312PCN21080 ()


  • Polymeric spinal interbody fusion cage
TLIF Cage 25mm x 16mm
Royal Oak Medical Devices LLC
TL251016-0001
In Commercial Distribution

  • 00812352020908 ()


  • Polymeric spinal interbody fusion cage
TLIF Cage 25mm x 14mm
Royal Oak Medical Devices LLC
TL251014-0001
In Commercial Distribution

  • 00812352020892 ()


  • Polymeric spinal interbody fusion cage
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