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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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C-C Blade, Left 180mm, Ø22
K2M, INC.
8030-90012
In Commercial Distribution

  • 10888857553590 ()
8030-90012

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 160mm, Ø22
K2M, INC.
8030-90010
In Commercial Distribution

  • 10888857553576 ()
8030-90010

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 140mm, Ø22
K2M, INC.
8030-90008
In Commercial Distribution

  • 10888857553552 ()
8030-90008

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 120mm, Ø22
K2M, INC.
8030-90006
In Commercial Distribution

  • 10888857553538 ()
8030-90006

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 100mm, Ø22
K2M, INC.
8030-90004
In Commercial Distribution

  • 10888857553514 ()
8030-90004

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 80mm, Ø22
K2M, INC.
8030-90002
In Commercial Distribution

  • 10888857553491 ()
8030-90002

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 210mm, Ø22
K2M, INC.
8030-90030
In Commercial Distribution

  • 10888857553774 ()
8030-90030

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 170mm, Ø22
K2M, INC.
8030-90026
In Commercial Distribution

  • 10888857553736 ()
8030-90026

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 120mm, Ø22
K2M, INC.
8030-90021
In Commercial Distribution

  • 10888857553682 ()
8030-90021

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 110mm, Ø22
K2M, INC.
8030-90020
In Commercial Distribution

  • 10888857553675 ()
8030-90020

  • Surgical retractor/retraction system blade, reusable
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