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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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CoRoent - 00887517812506

Interlock II Ti-C, 9x17x14mm 20°
Nuvasive, Inc.
6770920CP2
In Commercial Distribution

  • 00887517812506 ()


  • Polymeric spinal interbody fusion cage

Halyard - 20680651775102

ACMF ANGIO DRAPE BU 20
O&M HALYARD, INC.
77510
In Commercial Distribution

  • 20680651775102 ()
  • 30680651775109 ()


  • Patient surgical drape, single-use

Halyard - 20680651623601

HYH,FLTR,RESP,WH,-,20
O&M HALYARD, INC.
62360
Not in Commercial Distribution

  • 30680651623608 ()
  • 20680651623601 ()
  • 90680651623600 ()
62360

  • Surgical/medical face mask, non-antimicrobial, single-use

ALIF - 00887517836809

BASE Trial Rasp, 14x42x36mm 20°
Nuvasive, Inc.
6957058
In Commercial Distribution

  • 00887517836809 ()


  • Spinal implant trial

ALIF - 00887517836793

BASE Trial Rasp, 12x42x36mm 20°
Nuvasive, Inc.
6957057
In Commercial Distribution

  • 00887517836793 ()


  • Spinal implant trial

ALIF - 00887517836786

BASE Trial Rasp, 10x42x36mm 20°
Nuvasive, Inc.
6957056
In Commercial Distribution

  • 00887517836786 ()


  • Spinal implant trial

ALIF - 00887517836779

BASE Trial Rasp, 8x42x36mm 20°
Nuvasive, Inc.
6957055
In Commercial Distribution

  • 00887517836779 ()


  • Spinal implant trial

ALIF - 00887517836762

BASE Trial Rasp, 6x42x36mm 20°
Nuvasive, Inc.
6957054
In Commercial Distribution

  • 00887517836762 ()


  • Spinal implant trial

ALIF - 00887517836755

BASE Trial Rasp, 4x42x36mm 20°
Nuvasive, Inc.
6957053
In Commercial Distribution

  • 00887517836755 ()


  • Spinal implant trial

ALIF - 00887517836502

BASE Trial Rasp, 14x42x32mm 20°
Nuvasive, Inc.
6957028
In Commercial Distribution

  • 00887517836502 ()


  • Spinal implant trial
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