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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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TELIX K Ti Cage 11x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1136
In Commercial Distribution

  • 04250869607810 ()
109-015-1136

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 10x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1036
In Commercial Distribution

  • 04250869607803 ()
109-015-1036

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 9x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-0936
In Commercial Distribution

  • 04250869607797 ()
109-015-0936

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 8x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-0836
In Commercial Distribution

  • 04250869607780 ()
109-015-0836

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 7x36mm parallel
Biedermann Motech GmbH & Co. KG
109-031-0736
In Commercial Distribution

  • 04250869607773 ()
109-031-0736

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 15x32mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1532
In Commercial Distribution

  • 04250869607766 ()
109-015-1532

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 14x32mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1432
In Commercial Distribution

  • 04250869607759 ()
109-015-1432

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 13x32mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1332
In Commercial Distribution

  • 04250869607742 ()
109-015-1332

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 12x32mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1232
In Commercial Distribution

  • 04250869607735 ()
109-015-1232

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 11x32mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1132
In Commercial Distribution

  • 04250869607728 ()
109-015-1132

  • Metallic spinal interbody fusion cage
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