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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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Lordotic Scoring Trial, 10 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5628
In Commercial Distribution

  • 10840642121025 ()
10-5628

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 9 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5627
In Commercial Distribution

  • 10840642121018 ()
10-5627

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 8 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5626
In Commercial Distribution

  • 10840642121001 ()
10-5626

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 7 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5625
In Commercial Distribution

  • 10840642120998 ()
10-5625

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 6 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5624
In Commercial Distribution

  • 10840642120981 ()
10-5624

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 5 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5623
In Commercial Distribution

  • 10840642120974 ()
10-5623

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 10 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5614
In Commercial Distribution

  • 10840642120967 ()
10-5614

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 9 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5613
In Commercial Distribution

  • 10840642120950 ()
10-5613

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 8 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5612
In Commercial Distribution

  • 10840642120943 ()
10-5612

  • Polymeric spinal interbody fusion cage
Lordotic Scoring Trial, 7 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5611
In Commercial Distribution

  • 10840642120936 ()
10-5611

  • Polymeric spinal interbody fusion cage
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