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 15x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1536
In Commercial Distribution

  • 04250869607858 ()
109-015-1536

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 14x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1436
In Commercial Distribution

  • 04250869607841 ()
109-015-1436

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 13x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1336
In Commercial Distribution

  • 04250869607834 ()
109-015-1336

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 12x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1236
In Commercial Distribution

  • 04250869607827 ()
109-015-1236

  • Metallic spinal interbody fusion cage
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 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
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