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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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Arthrex® - 00888867252431

2-0 SC, 2.75, Str, w/FlushPort
ARTHREX, INC.
AR-11790F
In Commercial Distribution

  • 00888867252431 ()
AR-11790F

  • Suture cutter, reusable

BASE - 00887517703729

BASE Ti HL Implant, 14x38x36mm 20°
Nuvasive, Inc.
6959124
In Commercial Distribution

  • 00887517703729 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703712

BASE Ti HL Implant, 12x38x36mm 20°
Nuvasive, Inc.
6959123
In Commercial Distribution

  • 00887517703712 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703705

BASE Ti HL Implant, 10x38x36mm 20°
Nuvasive, Inc.
6959122
In Commercial Distribution

  • 00887517703705 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703170

BASE Ti HL Implant, 12x38x32mm 20°
Nuvasive, Inc.
6959068
In Commercial Distribution

  • 00887517703170 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703156

BASE Ti HL Implant, 8x38x32mm 20°
Nuvasive, Inc.
6959066
In Commercial Distribution

  • 00887517703156 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517703149

BASE Ti HL Implant, 6x38x32mm 20°
Nuvasive, Inc.
6959065
In Commercial Distribution

  • 00887517703149 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722461

BASE Ti HL Implant, 12x42x32mm 20°
Nuvasive, Inc.
6959178
In Commercial Distribution

  • 00887517722461 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722454

BASE Ti HL Implant, 10x42x32mm 20°
Nuvasive, Inc.
6959177
In Commercial Distribution

  • 00887517722454 ()


  • Metallic spinal interbody fusion cage

BASE - 00887517722447

BASE Ti HL Implant, 8x42x32mm 20°
Nuvasive, Inc.
6959176
In Commercial Distribution

  • 00887517722447 ()


  • Metallic spinal interbody fusion cage
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