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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 - 00887517809995

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

  • 00887517809995 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517810359

Interlock II, 16x17x14mm 20°
Nuvasive, Inc.
6771620
In Commercial Distribution

  • 00887517810359 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809872

Interlock II, 12x17x14mm 20°
Nuvasive, Inc.
6771220
In Commercial Distribution

  • 00887517809872 ()


  • Polymeric spinal interbody fusion cage

Modulus - 00887517020055

Modulus ALIF, 12x34x28mm 20°
Nuvasive, Inc.
1921032P2
In Commercial Distribution

  • 00887517020055 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517020048

Modulus ALIF, 10x34x28mm 20°
Nuvasive, Inc.
1921031P2
In Commercial Distribution

  • 00887517020048 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517020031

Modulus ALIF, 8x34x28mm 20°
Nuvasive, Inc.
1921030P2
In Commercial Distribution

  • 00887517020031 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517020024

Modulus ALIF, 6x34x28mm 20°
Nuvasive, Inc.
1921029P2
In Commercial Distribution

  • 00887517020024 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517019851

Modulus ALIF, 12x34x24mm 20°
Nuvasive, Inc.
1921012P2
In Commercial Distribution

  • 00887517019851 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517019844

Modulus ALIF, 10x34x24mm 20°
Nuvasive, Inc.
1921011P2
In Commercial Distribution

  • 00887517019844 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517019837

Modulus ALIF, 8x34x24mm 20°
Nuvasive, Inc.
1921010P2
In Commercial Distribution

  • 00887517019837 ()


  • Metallic spinal interbody fusion cage
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