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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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Anterior Cervical Cage W17 x D13 x H07, 4°
IMPLANET
380009
In Commercial Distribution

  • 03607503800099 ()
380009

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W17 x D13 x H06, 4°
IMPLANET
380008
In Commercial Distribution

  • 03607503800082 ()
380008

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W17 x D13 x H05, 4°
IMPLANET
380007
In Commercial Distribution

  • 03607503800075 ()
380007

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W17 x D13 x H04, 4°
IMPLANET
380006
In Commercial Distribution

  • 03607503800068 ()
380006

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H09, 4°
IMPLANET
380005
In Commercial Distribution

  • 03607503800051 ()
380005

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H08, 4°
IMPLANET
380004
In Commercial Distribution

  • 03607503800044 ()
380004

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H07, 4°
IMPLANET
380003
In Commercial Distribution

  • 03607503800037 ()
380003

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H06, 4°
IMPLANET
380002
In Commercial Distribution

  • 03607503800020 ()
380002

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H05, 4°
IMPLANET
380001
In Commercial Distribution

  • 03607503800013 ()
380001

  • Polymeric spinal interbody fusion cage
Anterior Cervical Cage W14 x D13 x H04, 4°
IMPLANET
380000
In Commercial Distribution

  • 03607503800006 ()
380000

  • Polymeric spinal interbody fusion cage
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