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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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TLX - 00887517824905

TLX Implant, 7x11x26mm 20°
Nuvasive, Inc.
1792601
In Commercial Distribution

  • 00887517824905 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517825179

TLX Implant, 12x11x31mm 20°
Nuvasive, Inc.
1792628
In Commercial Distribution

  • 00887517825179 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517825155

TLX Implant, 12x11x26mm 20°
Nuvasive, Inc.
1792626
In Commercial Distribution

  • 00887517825155 ()


  • Metallic spinal interbody fusion cage

TLX - 00887517825070

TLX Implant, 10x11x31mm 20°
Nuvasive, Inc.
1792618
In Commercial Distribution

  • 00887517825070 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517811875

Interlock II, 16x19x16mm 20°
Nuvasive, Inc.
6779620
In Commercial Distribution

  • 00887517811875 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811752

Interlock II, 15x19x16mm 20°
Nuvasive, Inc.
6779520
In Commercial Distribution

  • 00887517811752 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811516

Interlock II, 13x19x16mm 20°
Nuvasive, Inc.
6779320
In Commercial Distribution

  • 00887517811516 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811394

Interlock II, 12x19x16mm 20°
Nuvasive, Inc.
6779220
In Commercial Distribution

  • 00887517811394 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811295

Interlock II, 11x19x16mm 20°
Nuvasive, Inc.
6779120
In Commercial Distribution

  • 00887517811295 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811196

Interlock II, 10x19x16mm 20°
Nuvasive, Inc.
6779020
In Commercial Distribution

  • 00887517811196 ()


  • Polymeric spinal interbody fusion cage
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