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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 - 00887517810014

Interlock II, 13x17x14mm 25°
Nuvasive, Inc.
6771325
In Commercial Distribution

  • 00887517810014 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809995

Interlock II, 13x17x14mm 20°
Nuvasive, Inc.
6771320
In Commercial Distribution

  • 00887517809995 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517869692

Modulus TLIF-A, 14x9x30mm 8°
Nuvasive, Inc.
1149308P2
In Commercial Distribution

  • 00887517869692 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517869098

Modulus TLIF-A, 14x14x30mm 8°
Nuvasive, Inc.
1144308P2
In Commercial Distribution

  • 00887517869098 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517867490

Modulus TLIF-A, 14x11x34mm 8°
Nuvasive, Inc.
1141348P2
In Commercial Distribution

  • 00887517867490 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517862297

Modulus TLIF-A, 12x14x40mm 8°
Nuvasive, Inc.
1124408P2
In Commercial Distribution

  • 00887517862297 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517858696

Modulus TLIF-A, 11x14x40mm 8°
Nuvasive, Inc.
1114408P2
In Commercial Distribution

  • 00887517858696 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517858498

Modulus TLIF-A, 11x14x34mm 8°
Nuvasive, Inc.
1114348P2
In Commercial Distribution

  • 00887517858498 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517858474

Modulus TLIF-A, 11x14x34mm 15°
Nuvasive, Inc.
1114345P2
In Commercial Distribution

  • 00887517858474 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517858290

Modulus TLIF-A, 11x14x30mm 8°
Nuvasive, Inc.
1114308P2
In Commercial Distribution

  • 00887517858290 ()


  • Polymeric spinal interbody fusion cage
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