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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 Class Implantable

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CoRoent - 00887517993052

CoRoent LO Ti, 9x10x30mm 10°
Nuvasive, Inc.
6090930P2
In Commercial Distribution

  • 00887517993052 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517993045

CoRoent LO Ti, 9x10x25mm 10°
Nuvasive, Inc.
6090925P2
In Commercial Distribution

  • 00887517993045 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517993038

CoRoent LO Ti, 8x10x40mm 10°
Nuvasive, Inc.
6090840P2
In Commercial Distribution

  • 00887517993038 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517993021

CoRoent LO Ti, 8x10x35mm 10°
Nuvasive, Inc.
6090835P2
In Commercial Distribution

  • 00887517993021 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517993014

CoRoent LO Ti, 8x10x30mm 10°
Nuvasive, Inc.
6090830P2
In Commercial Distribution

  • 00887517993014 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517993007

CoRoent LO Ti, 8x10x25mm 10°
Nuvasive, Inc.
6090825P2
In Commercial Distribution

  • 00887517993007 ()


  • Metallic spinal interbody fusion cage

Modulus - 00887517991973

Modulus TLIF-O Implant Set - Outlier 2
Nuvasive, Inc.
MDLUSTLIFOOUTIMP2
In Commercial Distribution

  • 00887517991973 ()


  • Device sterilization/disinfection container, reusable

Modulus - 00887517991966

Modulus TLIF-O Implant Set - Outlier 1
Nuvasive, Inc.
MDLUSTLIFOOUTIMP1
In Commercial Distribution

  • 00887517991966 ()


  • Device sterilization/disinfection container, reusable

Modulus - 00887517991942

Modulus TLIF-O Implant Set - Core
Nuvasive, Inc.
MDLUSTLIFOCOREIMP
In Commercial Distribution

  • 00887517991942 ()


  • Device sterilization/disinfection container, reusable

Cohere - 00887517984067

COHERE XLXW, 8x26x60mm 0°
Nuvasive, Inc.
8267860P2
In Commercial Distribution

  • 00887517984067 ()


  • Polymeric spinal interbody fusion cage
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