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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, Right 180mm, Ø22
K2M, INC.
8030-90027
In Commercial Distribution

  • 10888857553743 ()
8030-90027

  • 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 150mm, Ø22
K2M, INC.
8030-90024
In Commercial Distribution

  • 10888857553712 ()
8030-90024

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 130mm, Ø22
K2M, INC.
8030-90022
In Commercial Distribution

  • 10888857553699 ()
8030-90022

  • 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 100mm, Ø22
K2M, INC.
8030-90019
In Commercial Distribution

  • 10888857553668 ()
8030-90019

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 80mm, Ø22
K2M, INC.
8030-90017
In Commercial Distribution

  • 10888857553644 ()
8030-90017

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 210mm, Ø22
K2M, INC.
8030-90015
In Commercial Distribution

  • 10888857553620 ()
8030-90015

  • 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
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