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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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LOCK SHAFT INSERTER
SPINEFRONTIER, INC.
SI50001
In Commercial Distribution

  • 00190361037842 ()


  • Polymeric spinal interbody fusion cage
INSERTER, LOCK SHAFT, SLAP HAMMER
SPINEFRONTIER, INC.
11-50264
In Commercial Distribution

  • 00190361037835 ()


  • Polymeric spinal interbody fusion cage
Inserter, Assembly, Dorado T-LIFT
SPINEFRONTIER, INC.
11-05000
In Commercial Distribution

  • 00190361037828 ()


  • Polymeric spinal interbody fusion cage
T-LIFT Inline Inserter, 14 Deg
SPINEFRONTIER, INC.
13-05002
In Commercial Distribution

  • 00190361037811 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 14 mm
SPINEFRONTIER, INC.
SI02861-07
In Commercial Distribution

  • 00190361037798 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 13 mm
SPINEFRONTIER, INC.
SI02861-06
In Commercial Distribution

  • 00190361037781 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 11 mm
SPINEFRONTIER, INC.
SI02861-04
In Commercial Distribution

  • 00190361037767 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 9 mm
SPINEFRONTIER, INC.
SI02861-02
In Commercial Distribution

  • 00190361037743 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 8 mm
SPINEFRONTIER, INC.
SI02861-01
In Commercial Distribution

  • 00190361037736 ()


  • Polymeric spinal interbody fusion cage
25mm T-LIFT Straight Trial, 6 mm
SPINEFRONTIER, INC.
SI02861-09
In Commercial Distribution

  • 00190361037712 ()


  • Polymeric spinal interbody fusion cage
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