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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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ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 16mm
SPINECRAFT, LLC
A7100-16
In Commercial Distribution

  • M824A7100161 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 3 1X 14mm
SPINECRAFT, LLC
A7100-14
In Commercial Distribution

  • M824A7100141 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 12mm
SPINECRAFT, LLC
A7100-12
In Commercial Distribution

  • M824A7100121 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 10mm
SPINECRAFT, LLC
A7100-10
In Commercial Distribution

  • M824A7100101 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 15 X 34mm
SPINECRAFT, LLC
L7810-15-034
In Commercial Distribution

  • M824L7810150341 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 15 X 32mm
SPINECRAFT, LLC
L7810-15-032
In Commercial Distribution

  • M824L7810150321 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 15 X 30mm
SPINECRAFT, LLC
L7810-15-030
In Commercial Distribution

  • M824L7810150301 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 15 X 28mm
SPINECRAFT, LLC
L7810-15-028
In Commercial Distribution

  • M824L7810150281 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 14 X 34mm
SPINECRAFT, LLC
L7810-14-034
In Commercial Distribution

  • M824L7810140341 ()


  • Polymeric spinal interbody fusion cage
ORIO-TL STRAIGHT TLIF CAGE, GEN II, 10mm WIDE, 10 X 14 X 32mm
SPINECRAFT, LLC
L7810-14-032
In Commercial Distribution

  • M824L7810140321 ()


  • Polymeric spinal interbody fusion cage
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