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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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21X27 TRIAL HEAD, ARENA-L ALLO, 19MM
SPINEFRONTIER, INC.
11-82002-19
In Commercial Distribution

  • 00190361039204 ()


  • Polymeric spinal interbody fusion cage
21X27 TRIAL HEAD, ARENA-L ALLO, 15MM
SPINEFRONTIER, INC.
11-82002-15
In Commercial Distribution

  • 00190361039181 ()


  • Polymeric spinal interbody fusion cage
21X27 TRIAL HEAD, ARENA-L ALLO, 11MM
SPINEFRONTIER, INC.
11-82002-11
In Commercial Distribution

  • 00190361039167 ()


  • Polymeric spinal interbody fusion cage
21X27 TRIAL RASP HEAD, ARENA-L ALLO, 21MM
SPINEFRONTIER, INC.
11-82001-21
In Commercial Distribution

  • 00190361039143 ()


  • Polymeric spinal interbody fusion cage
21X27 TRIAL RASP HEAD, ARENA-L ALLO, 15MM
SPINEFRONTIER, INC.
11-82001-15
In Commercial Distribution

  • 00190361039112 ()


  • Polymeric spinal interbody fusion cage
21X27 TRIAL RASP HEAD, ARENA-L ALLO, 11MM
SPINEFRONTIER, INC.
11-82001-11
In Commercial Distribution

  • 00190361039099 ()


  • Polymeric spinal interbody fusion cage
7MM 21X27 TRIAL, ARENA-L ALLO
SPINEFRONTIER, INC.
11-82005
In Commercial Distribution

  • 00190361039075 ()


  • Polymeric spinal interbody fusion cage
7MM 21X27 TRIAL RASP, ARENA-L ALLO
SPINEFRONTIER, INC.
11-82004
In Commercial Distribution

  • 00190361039068 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 38X28 Lordotic 12°, 17L
SPINEFRONTIER, INC.
11-81043-17
In Commercial Distribution

  • 00190361039051 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 38X28 Lordotic 12°, 15L
SPINEFRONTIER, INC.
11-81043-15
In Commercial Distribution

  • 00190361039044 ()


  • Polymeric spinal interbody fusion cage
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