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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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CURETTE EX0413053 BAYONET PUSH 5.2MM
MEDTRONIC SOFAMOR DANEK, INC.
EX0413053
In Commercial Distribution

  • 00643169350984 ()


  • Bone curette, reusable
CURETTE EX0413052 BAYONET PUSH 3.6MM
MEDTRONIC SOFAMOR DANEK, INC.
EX0413052
In Commercial Distribution

  • 00643169350977 ()


  • Bone curette, reusable
CURETTE EX0413051 BAYONET PUSH 1.8MM
MEDTRONIC SOFAMOR DANEK, INC.
EX0413051
In Commercial Distribution

  • 00643169350960 ()


  • Bone curette, reusable
AWL X0413023 LARGE W/ BALL HANDLE
MEDTRONIC SOFAMOR DANEK, INC.
X0413023
In Commercial Distribution

  • 00643169349575 ()


  • Bone awl, reusable
Angled Stirrup Curette
K2M, INC.
AG01-96031
In Commercial Distribution

  • 10888857422858 ()
AG01-96031

  • Bone curette, reusable
Straight Curette, Down, Size #4
K2M, INC.
AG01-96030
In Commercial Distribution

  • 10888857422841 ()
AG01-96030

  • Bone curette, reusable
Angled Curette, Up, Size #4
K2M, INC.
AG01-96028
In Commercial Distribution

  • 10888857422827 ()
AG01-96028

  • Bone curette, reusable
Angled Curette, Up, Size #2
K2M, INC.
AG01-96027
In Commercial Distribution

  • 10888857422810 ()
AG01-96027

  • Bone curette, reusable
Forward Curette (Long), Size #2
K2M, INC.
AG01-96012
In Commercial Distribution

  • 10888857422797 ()
AG01-96012

  • Bone curette, reusable
Curette, Size #4
K2M, INC.
AG01-96011
In Commercial Distribution

  • 10888857422780 ()
AG01-96011

  • Bone curette, reusable
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