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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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S-LIFT® - 00190361037910

TRIAL, STRAIGHT, 22MM WIDE, 4MM
SPINEFRONTIER, INC.
11-50250-04
In Commercial Distribution

  • 00190361037910 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037903

ADJUSTMENT COLLAR, S-LIFT INSERTER
SPINEFRONTIER, INC.
14-50002
In Commercial Distribution

  • 00190361037903 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037897

INSERT HOLDER ASSEMBLY, S-LIFT INSERTER
SPINEFRONTIER, INC.
14-50001
In Commercial Distribution

  • 00190361037897 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037880

LOCKING ROD ASSEMBLY, S-LIFT INSERTER
SPINEFRONTIER, INC.
14-50000
In Commercial Distribution

  • 00190361037880 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037873

OUTER SLEEVE ASSEMBLY
SPINEFRONTIER, INC.
SI50003
In Commercial Distribution

  • 00190361037873 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037866

IMPLANT HOLDER, INSERTER
SPINEFRONTIER, INC.
SI50002
In Commercial Distribution

  • 00190361037866 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037859

INSERTER, IMPLANT HOLDER, SLAP HAMMER
SPINEFRONTIER, INC.
11-50265
In Commercial Distribution

  • 00190361037859 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037842

LOCK SHAFT INSERTER
SPINEFRONTIER, INC.
SI50001
In Commercial Distribution

  • 00190361037842 ()


  • Polymeric spinal interbody fusion cage

S-LIFT® - 00190361037835

INSERTER, LOCK SHAFT, SLAP HAMMER
SPINEFRONTIER, INC.
11-50264
In Commercial Distribution

  • 00190361037835 ()


  • Polymeric spinal interbody fusion cage

T-LIFT® - 00190361037828

Inserter, Assembly, Dorado T-LIFT
SPINEFRONTIER, INC.
11-05000
In Commercial Distribution

  • 00190361037828 ()


  • Polymeric spinal interbody fusion cage
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